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From Tools 2 Succeed, Inc
Time Management Webinar

Do you know the difference between the urgent and the important?
Do you make time for the important?
Most people go through life by default; learn to live your life by design!
In our interactive Time Management webinar, you will learn:
* How you are currently using your time
* The barriers which keep you from managing your time more effectively
* The difference between important and
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From Statistics & Analytics Consultants Group
Introduction to Surveys





This course is an introduction to survey design, methodology, implementation and execution. The course will also go through questionnaire design/ writing, sample design, data collection strategies, multivariate analyses, and presentation of tables/ graphs. For more information contact us directly.
Our courses are offered in three formats a resident course at our office, a corporate course on
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From Sql Server Online Training
SQL DBA Online Trainings with Case Studies







Realtime SQL Server and DBA Online Training is provided with LIVE databases and Case Studies.
SQL SERVER Administration [SQL DBA] Course Contents:
SQL Server basics and T-SQL:
SQL Server Design Architecture
Database Design and Table Design Principles
Compression Techniques and Capacity Planning
Data Integrity & Consistency
Views and Data Security
JOINS and Sub Queries and Query
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From Requirements Solutions Group
How to Analyze and Improve Business Data




Using business data model to identify potential business problems that are caused by missing or improperly defined business data is the next step in the progression from dataa asa aa problem to dataa asa aa valuablea resource.
This on-line business analyst training workshop assumes you know how to draw business data models (entity/ relationship diagrams). It is designed to give you a
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How to Write Effective Business Requirements




Writing effective business requirements is a critical skill for subject matter experts who represent the business interests on an IT project and for business analysts. The challenge lies in defining business needs in the form of business requirements, stakeholder requirements, solution requirements, and transition requirements that other audiences will interpret as intended and use to design the
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From Spectralight Images, LLC
3DS MAX Online - Lighting and Rendering with Photometric Lights



This online course will take you through the process of lighting your scene using photometric lights in 3DS MAX & Design 2010. In this course you will learn how to set up and configure lighting for your scene, learn the parameters associated with photometric lights and use IES data to enhance the realism of the lights in your scene.
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3DS MAX Online - Rendering with Mental Ray


For most forms of animation, rendering an image the the most critical step in the process. This online course will take you through the various options available when using Mental Ray to render in 3DS MAX & Design 2010. You will learn about the options available for optimizing render time and image quality, using indirect illumination and working with several new features available in release
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3DS MAX Online - Mapping Techniques


Whether you are building a tank or a brick wall, placement of texture maps is critical to the appearance of your finished model. Learn to use the tools and interface in 3DS MAX 2010 to apply texture maps to objects in your scenes. You will learn how to use the UVW mapping modifier, and the Unwrap UVW modifier in order to apply custom mapping to objects in your scene.
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3DS MAX Online - Material Creation Using Mental Ray Arch Design


This online course will take you through the various options available for the creation of materials using the Mental Ray Arch and Design material in 3DS MAX & Design 2010. You will learn about how to use the many options and how they work together to build a variety of materials from simple plastic to unique and complex surfaces.
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3DS MAX Online - Fundamentals of Modeling 1


Modeling is the foundation for creating your world inside of 3DS MAX. This online course will take you through the use of the modeling tools and interface you will use to build objects and scenes. This course will take you through the creation of spline objects, using the modifier stack, and editing spline objects.
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3DS MAX Online - Fundamentals of Modeling 2


3D Modeling allows you to create anything your imagination can dream up. This online course will take you through the use of the modeling tools and interface you will use to build objects and scenes. This course will take you through the creation of 3 dimensional primitive objects, the use of proboolean and introduce basic poly modeling techniques.
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Maya Online - Fundamentals of Maya


Based on the Autodesk Maya fundamentals standards, this course provides an introduction to Maya 2009, one of the favorite animation tools of Hollywood. Autodesk Maya 2009 is a powerful program that can be challenging to learn and master. This course provides an introduction to Autodesk Maya 2009 that will help new users make the most of this application, and expand the abilities of existing,
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3DS MAX Online - Fundamentals of 3DS MAX


Based on the Autodesk 3DS MAX fundamentals standards, this course provides an introduction to one of the most popular 3D animation programs on the planet. Autodesk 3ds Max Design is a powerful program that can be challenging to learn and master. This course provides an introduction to Autodesk 3ds Max/ Design 2010 that will help new users make the most of this application, and expand the abilities
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From Black Box Consulting
Xilinx FPGA Academy I - Introduction



The Xilinx Academy I is a 5 day course designed for new to beginner Xilinx FPGA users such as graduates, digital Engineers moving to FPGAs or Software engineers taking the plunge with no, or no more than 0-12 months experience with FPGAs and VHDL. It is also a good course to gain a structured understanding of VHDL.
We talk you through the ISE tool and its capabilities, the implementation flow,
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Designing with the Xilinx Spartan-6 FPGA
Are you interested in learning how to effectively utilize Spartan ®-6 FPGA architectural resources? This course supports both experienced and less experienced FPGA designers who have already completed the Essentials of FPGA Design course. This course focuses on understanding as well as how to properly design for the primary resources found in this popular device family.
Topics covered
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Designing with Xilinx Virtex-6 FPGAs



Are you interested in learning how to effectively utilize Virtex ®-6 FPGA architectural resources? This course supports both experienced and less experienced FPGA designers who have already completed the Essentials of FPGA Design course. This course focuses on understanding as well as how to properly design for the primary resources found in this popular device family.
Topics covered
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Designing with Multi-Gigabit Serial IO in Xilinx FPGAs
Learn how to employ RocketIO GTP and GTX serial transceivers in your Spartan ®-6 LXT or Virtex ®-6 FPGA design. Understand and utilize the features of the RocketIO transceiver blocks, such as 8B/ 10B and 64B/ 66B encoding, channel bonding, clock correction, and comma detection. Additional topics include use of the Architecture Wizard, synthesis and implementation considerations, board
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Designing a Xilinx FPGA LogiCore PCI Express System
Attending the Designing a LogiCORE PCI Express System will provide you a working knowledge of how to implement a Xilinx PCI Express ® core in your applications. This course focuses on the implementation of a Xilinx PCI Express system with supporting logic & example designs. With this experience, you can improve your time to market with your PCIe core design. Various Xilinx PCI Express core
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Xilinx FPGA Academy III - Advanced



This 5 day course is targeted towards designers with a good few projects under their belts.
It discusses advanced features, options and techniques. From User Constraints syntax, source and system sycnhronous IO timing contraints, TCL scripting, FPGA Editor.
There are 2 days indepth training on using Plan ahead for Timing closure, area constraints, IP reuse, compression and run time
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Xilinx FPGA Academy II - Intermediate



This 5 day course is for designers with a few projects under their belt to the experienced.
Here we get insdie the FPGA and get you thinking about what you right in code and what gets created in actual hardware. This thought process is the foundation of a good designer.
We address the Slice in indepth detail, we discuss memory types, carry chains, LUTs, synchronous design techniques, using
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From Relevant Trafik
WordPress Training 1 Video Conference

Relevant Trafik is an award winning Search Marketing and Design firm. We specialize in Social Media Marketing, Design/ Development and Training. We train on how to use the most popular blogging platform: WordPress. WordPress can be used as a blog or as a full blown website, giving you the user, the advantage of controlling your identity and your brand. WordPress is a free and open source software
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From Kogent
BOC310 - Crystal Reports - Report Design I - Fundamentals of Report Design - Virtual Session
BOC310: Crystal Reports - Report Design I - Fundamentals of Report Design - Virtual Session
Crystal Reports 2008 is a powerful, dynamic, actionable reporting solution that helps you design, explore, visualize, and deliver reports via the web or embedded in enterprise applications. This two-day instructor-led course is designed to give you comprehensive skills and in-depth knowledge to plan and
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BOW310 - BusinessObjects Web Intelligence XI 30 Report Design - Virtual Class
BOW310: BusinessObjects Web Intelligence XI 30 Report Design - Virtual Class
This two-day instructor-led course is designed to give you the comprehensive skills and in-depth knowledge needed to access, analyze and share data using BusinessObjects InfoView and BusinessObjects Web Intelligence. During this course, you'll learn how to organize, manage and distribute documents using InfoView.
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BOW320 - BusinessObjects Web Intelligence XI 30 - Advanced Report Design - Virtual Class
BOW320: BusinessObjects Web Intelligence XI 30 - Advanced Report Design - Virtual Class
BusinessObjects Web Intelligence is a query, reporting and analysis tool that allows you to access the data in your corporate databases directly from within BusinessObjects Enterprise InfoView and to present and analyze this information in a Web Intelligence document. This one-day instructor-led classroom
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From RAMCO Software Training
Online Training
We have taken our proven methodology from the live classroom environment to the virtual classroom with our new E-learning curriculum and online delivery style. Live or recorded, online training is now available for open enrollment and private groups with specific training needs. E-learning courses for Microsoft Office include Excel Basics, Charts, PivotTables, and Formulas and Functions.
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From TypeLabs
TypeLabs presents Making Type Training Experiential with Hile Rutledge

In this program, Hile Rutledge of OKA will detail a number of training ideas, processing techniques and group exercises designed to expand a trainera s options in working with groups. Including a review of frequently asked questions in type training and a frank discussion of a what ifsa (the dreaded mistakes and unexpected exercise outputs that can arise when drawing on group
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TypeLabs presents Driving Team Performance from the Inside Out with Susan Nash

Building effective real and virtual team dynamics is a vital factor in 21st century organizational success. This program will show how the theories of temperament and psychological type can be applied to raising team productivity. Participants will learn how to create and diagnose a team profile of temperaments, functions and attitudes, and type. This profile will be used to comprehend team
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From Global Innovative Campus
Design and Manufacture of Machine Elements Refresher Workshop 36 PDHs
Design and Manufacture of Machine Elements Refresher Workshop (36 PDHs)
Course Code: 07-Mec-A4
Date: 01 Sep - 31 Dec 2012
Location: Distance
Details: This workshop is available through distance education, start and end date is open throughout the year.
Distance education link:
http://gic-edu. com/ examprep. aspx
Course Description:
This course is been designed to train the P.
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From Single Sourcing Solutions, Inc
Configuring the Arbortext Application Tutoring





A customized version of the "Configuring the Arbortext Application" course, this mentor-led, one-on-one, individual instruction is tailored to the needs of the student and focused on their individual, personal skill development.
This course emphasizes hands-on experience, interaction between student and mentor, in a tutoring-like environment. Although the course is compressed, you will develop
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From Future Media Concepts
Avid Media Composer Effects Techniques v35 - Online 2 days
Students learn to design multilayered and multi-nested effects on Avid Media Composer for maximum quality and optimal render time. Hands-on exercises help students create and combine effects to achieve real-world results.
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Fast Track to ColdFusion 8 - Online
Fast Track to ColdFusion 8 is a course that provides experienced Web developers with the knowledge and hands-on practice they need to start building and maintaining dynamic and interactive Web applications using ColdFusion 8.
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Flash Complete - Online
lash is one of the most engaging and innovative, and versatile applications available - allowing the creation of pretty much anything from simple slideshows, animated banners and icons and cartoons, to Rich Internet Applications, Interactive videos, and Dynamic User Interfaces for web sites, kiosks, etc. The possibilities are endless, except that now, it just got better. In 2009, Adobe released
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ActionScript 30 for Adobe Flash Professionals - Online
ActionScript 3. 0 for Adobe Flash Professionals provides experienced Flash designers with the knowledge and hands-on practice they need to create dynamically generated event-driven animation and interactive games with Flash. The course teaches fundamental programming techniques. It begins by introducing core concepts including instance names, variables, functions, properties, and methods; then
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Dreamweaver Complete - Online
Dreamweaver Complete provides web designers with the knowledge and hands-on practice they need to build and manage professional websites using Dreamweaver CS5.
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Adobe RoboHelp 7 - Online
Do you want to create a help system for an application? Maybe you're part of a documentation services team, and would like to enhance the appearance and functionality of help systems using advanced techniques. Learn to use Adobe RoboHelp 7, the authoring tool with advanced features that assists you in creating such projects. In this course, you will work with RoboHelp to create an advanced help
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Photoshop Complete - Online
This 3-day course provides a thorough overview of the interface, the tools, the features, tricks, and tips for using Photoshop CS4. The course is an ideal combination of instructor-led demonstration and hands-on practice.
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Photoshop Advanced Print and Photography - Online
This 2-day course provides a thorough overview for experienced users who wish to further their effectiveness on Photoshop. The course trains photographers and designers how to catalogue their work as well as how to enhance their photographs. Because this class is aimed mainly at Photographers and artists who work with photographs, we have included Lighroom and Camera RAW in the lessons. This
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Photoshop Web and Video - Online
This 2-day course provides a thorough overview for experienced users who wish to further their effectiveness on Photoshop. This class is aimed at the Photoshop professional who needs to enhance their knowledge to work with web and video images more effectively. The course is an ideal combination of instructor-led demonstration and hands-on practice.
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InDesign Complete - Online
Adobe InDesign software speaks the language of professional designers, delivering unparalleled creative freedom, productivity, and precision for designing superb pages. It works seamlessly with Adobe Photoshop and Adobe Illustrator, providing a single integrated design environment that doesn't interrupt your creative process. InDesign even opens Quark XPress and Adobe PageMaker files, so you can
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Illustrator Complete - Online
Adobe Illustrator CS4 software is an essential design tool for anyone who needs to express ideas visually in print, on the Web, and in any other medium. This course provides a thorough overview of the interface, the tools, the features, tricks and tips for using Illustrator CS4. The course is an ideal combination of instructor-led demonstration and hands-on practice.
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Adobe Acrobat Complete - Online
Acrobat's cross-platform capabilities allow you to distribute your documents efficiently without sacrificing the original design. When you need to distribute your documents to viewers using a variety of platforms and software - Acrobat is your tool of choice. This three-day course provides an excellent overview of how to convert your work into Adobe Portable Document Format (PDF). You will learn
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From Klee Associates (ERPtips)
SAP ABAP Programming Training

SAP ABAP Programming teaches you an overview of the basic concepts and architecture of SAP ABAP. You will also get hands-on experience working with SAP ABAP, including how to design and create performance-optimized programs, ALV, graphical display and Dynamic Documents, how to generate output using charts, RFCs, Enhancement and Switch framework, and much more.
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From NR Computer Learning Center
Interactive Analytics
This Free Webinar is designed for Business analysts and developers to become familiar with using BIRT to design and develop Interactve Financial Dashboards and BI Applications with rich data visualizations. BIRT is a top level project within Eclipse and is the fastest growing open source reporting technology with over 5 million dowloads in the past 2 years. Actuate founded and continues to co-lead
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From Webucator
Introduction to Xcelsius 2008 Training
This Xcelsius training class will serve as an introduction to building dashboards with Xcelsius 2008. Students will create, design, and publish business dashboards using the Xcelsius application.
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Web Design and Usability Techniques
For many new or intermediate Web designers, it
'
s difficult to know where to start when designing a site. It
'
s easy to make the mistake of assuming that the functionality of a site will take shape over time, or the design will fall into place as you build the site. This web usability training class provides guidance in how to plan and design functional, successful web sites.
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SharePoint Designer Training
SharePoint Designer is based on FrontPage technologies. It is a superset of Expression Web, which is also based on FrontPage. In addition to the web development features included in Expression Web, SharePoint Designer includes features specific to SharePoint, such as the ability to create, open, edit, backup and restore SharePoint sites and to create SharePoint master pages and web part pages.
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Object-Oriented Analysis and Design (OOAD) Training with UML
This Object-Orientated Analysis and Design (OOAD) with UML training course teaches students how to use object-oriented techniques from requirements gathering to implementation. Learn how to analyze and design classes and their relationships to each other in order to build a model of the business requirements. All the UML diagrams are covered in this OOAD class to identify the most suitable diagram
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MOC 8399 - FRx 6.7 Report Design Essentials I
This Microsoft FRx training class covers the basic report design skills you need to create, maintain and distribute presentation quality reports using Microsoft FRx. The class also includes coverage of additional functionality designed to help you create new reports, and distribute and analyze your company
'
s financial information. You learn about basic foundational skills, complex calculations,
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MOC 8400 - FRx 6.7 Report Design Essentials II
This advanced Microsoft FRx training class builds on the basic report design skills learned in MOC8399. Using Microsoft FRx you learn advanced report design including linking to external worksheet data, linking row formats, multi company consolidations, currency translation reporting and cash flow. A combination of instructor guided exercises and practice tutorials allow students to master their
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MOC 6294 - Planning and Managing Windows 7 Desktop Deployments and Environments
This Windows 7 training class is intended for desktop administrators who want to specialize in desktop deployment, configuration, and management . In this Windows 7 course, students will learn how to plan and deploy Windows 7 desktops in large organizations . They will also learn how to design, configure, and manage the Windows 7 client environment. This Windows 7 course helps students prepare for
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MOC 3938 - Updating Your Skills from Microsoft Exchange 2000 Server or Microsoft Exchange Server 2003 to Microsoft Exchange Serv
This Microsoft Exchange training class targets Microsoft Exchange 2000 Server or Microsoft Exchange Server 2003 administrators who need to upgrade their skills to manage a Microsoft Exchange Server 2007 infrastructure. This class focuses on the new features and administrative tasks in Exchange Server 2007.Students will learn skills that enable them to deploy and manage an Exchange Server 2007
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Intermediate Java Training
This course teaches programming in the Java language -- i.e. the Java Standard Edition platform. It is intended for students with previous Java experience or training, who already know the fundamentals of the Java architecture and basic procedural programming. This course provides in-depth coverage of object-oriented concepts and how to apply them to Java software design and development. The
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Fireworks CS4 Training: Drawing and Composites
In this Adobe Fireworks training class, students receive a comprehensive introduction to using Fireworks CS4 to design and create graphics.
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Fireworks CS4 Training: Web Integration
In this Adobe Fireworks training class, students learn to create graphics for the Web and to use Fireworks in in their web design.
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Introduction to Microsoft Expression Web Design
This Expression Web training course is for students interested in learning Microsoft Expression Web to design attractive, CSS-based, scalable web sites and front-ends for web-based applications.
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Introduction to Microsoft Expression Web Design and Development
This Expression Web training course is for students interested in learning Microsoft Expression Web to design attractive, CSS-based, scalable web sites and front-ends for web-based applications. It also includes an introduction to working with ASP.NET in Expression Web.
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Introduction to Crystal Reports 2008 Training
This Crystal Reports training class is designed for new users of Crystal Reports 2008. Some of the topics covered include a review of the software features, report design and the creation of presentation quality reports. Students get practical experience through plenty of hands-on exercises.
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Intermediate Crystal Reports 2008 Training
This Crystal Reports training class is designed to enhance your basic report writing skills and move you into creating more complex reports. Time will be spent walking you through the tips and tricks of advanced report writing along with a good amount of hands on practice. In addition, you will cover professional design, techniques, sub-reporting and advanced formulas.
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Advanced Adobe Captivate 4 Training
In this advanced Captivate training class, you will learn Captivate
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s higher-end functionality while improving your production skills via project templates, design templates, advanced actions and scripts. You will learn to collaborate with team members via Captivates
'
powerful commenting features. You
'
ll enhance your users experience via variables that will make it seem like each eLearning
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C++ Training
This C++ training class teaches students to design and write programs in the C++ language, emphasizing object-oriented approaches to designing solutions.
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MySQL Database Design
The MySQL training course targets new or existing users of MySQL with some
experience with relational database management systems. The MySQL course
covers database design theory and several essential elements of MySQL
database in general.
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SQL Server 2005 Analysis Services (SSAS) Training
In this SSAS training course, you will learn how to use Microsoft SQL Server 2005 Analysis Services (SSAS) to design and implement OnLine Analytical Processing (OLAP) cubes and data mining models to support Business Intelligence (BI) solutions.This SSAS course includes concepts, procedures and practices based on real-world experience giving both the novice and experienced SQL Server 2005 developer
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MOC 6234 - Implementing and Maintaining Microsoft SQL Server 2008 Analysis Services
This SSAS training class teaches students how to implement an Analysis Services solution in an organization. The class discusses how to use the Analysis Services development tools to create an Analysis Services database and an OLAP cube, and how to use the Analysis Services management and administrative tools to manage an Analysis Services solution.This SSAS class targets people who design and
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MOC 5061 - Implementing Microsoft Office SharePoint Server 2007
This SharePoint training class provides students with the knowledge and skills required to implement Microsoft Office SharePoint Server 2007 successfully in their organization.The audience for this class is Business Application Administrators (BAAs), Web Administrators and Server Administrators who are engaged in the planning, design, and selection of line-of-business (LOB) applications (including
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From GlobalCompliancePanel
Verification vs Validation in Regulated Industries - Webinar By GlobalCompliancePanel
Overview: Attend this webinar to understand the differences and benefits of verification and validation. Learn about the risks and complications involved with the application of sound verification and validation principles.
Thursday, March 1, 2012
10: 00 AM PST | 01: 00 PM EST
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Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine
Overview: The FDA QSR and the Medical Device Directive specify certain documents or records that should be included in your organization's quality systems - Design History File (DHF), the Device Master Record (DMR) the Device History Record (DHR), and the Technical File (TF).
Tuesday, February 14, 2012
10: 00 AM PST | 01: 00 PM EST
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Reusable Device Cleaning Disinfection and Sterilization Validations Overview and Key Design Considerations for Device Engineers
Validation of reusable medical devices requires that the manufacturer develop methods for cleaning (after use) washing to remove all foreign matter possibly disinfecting and repackaging for the next use.
The diversity of medical devices their intended use and classification in accordance with the food and drug administration requires that the manufacturer develop and validate the reprocessing
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Lyophilization Process Development and Cycle Design with a Case Study - Webinar By GlobalCompliancePanel
This webinar will cover the process and benefits of using an empirical approach to design an optimized lyophilization cycle.
Wednesday, January 11, 2012
10: 00 AM PST | 01: 00 PM EST
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Excel Spreadsheet Validation for FDA 21 CFR Part 11 - Webinar By GlobalCompliancePanel
This webinar will describe the regulatory and business requirements for Excel spreadsheets, using examples from FDA recommendations. It will then cover the design and installation of those Excel Spreadsheets, to ensure the integrity of the data, and will discuss how to ensure 21 CFR 11 compliance during the development, installation and maintenance of a spreadsheet application.
Tuesday,
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DHF DMR DHR and the Technical File-Design Dossier - Similarities and Differences - Webinar By GlobalCompliancePanel
This webinar will examine the existing and proposed requirements for the FDA's DHF -- including its derivative documents, the DMR and DHR.
Wednesday, March 7, 2012
10: 00 AM PST | 01: 00 PM EST
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Change Control Management From Design to Commercialization - Webinar By GlobalCompliancePanel
There is a need to implement an adequate formal level of change control during engineering projects (referred to as an Engineering Change Control) after the approval of the equipment/ systems specifications in addition to the more formal change control after the qualification of these systems.
Thursday, January 12, 2012
10: 00 AM PST | 01: 00 PM EST
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Risk Management in IEC 60601-1 Third Edition - Webinar By GlobalCompliancePanel
IEC 60601-1 Third Edition was released in late 2005. It is a new philosophy in standards for medical electrical devices to accommodate rapid advances in technology.
This new philosophy has been difficult for test houses and compliance bodies to absorb and develop test strategies. Currently, the EU and Canada have announced May 31-June 1, 2012 as the date when the Second Edition will be
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New Process Validation Life-Cycle Approach - Apply statistical tools to demonstrate Process Capability - Webinar By GlobalCompli
This webinar will describe the new Process Validation Life-Cycle Approach as defined in the revised FDA guideline. The three stages will be described in detail including: Process Design, Process Qualification and the Continued Process Verification.
Thursday, December 15, 2011
10: 00 AM PST | 01: 00 PM EST
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Design History File DHF the Device Master Record DMR and the Device History Record DHR Principles on Lean Documents and Lean Co
Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR) are key building blocks used in the design, development, manufacturing, and cGMP compliance for the Medical Device Industry.
Tuesday, December 13, 2011
10: 00 AM PST | 01: 00 PM EST
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Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration - Webinar By GlobalComp
Design Inputs, Design Outputs, and Traceability matrices present a challenge to almost all industries that apply design controls.
Tuesday, November 22, 2011
10: 00 AM PST | 01: 00 PM EST
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Designing and Conducting Effective Structured Interviews - Webinar By TrainHR
This webinar will cover the process of determining the right questions to predict success on the job, including questions to determine a cultural match to the organization, how to design a program with the advantages of structured interviews and elimination of the disadvantages some programs have
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Using Statistics in Compensation - Webinar By TrainHR
This webinar will address the statistics behind pay program design and administration, from the design of pay structures through the analysis of pay survey data. It will explore how practitioners create and analyze pay ranges, pay survey data, individual and group pay rates, and other elements of a compensation program.
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Risk Management during device design according to ISO14971 - Webinar By GlobalCompliancePanel
Learn how to put an effective risk management plan in place and fulfill the requirements of ISO14971.
Thursday, October 6, 2011
10: 00 AM PDT | 01: 00 PM EDT
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The DHF DMR DHR and the Technical File Design Dossier - Regulatory Requirements - Webinar By GlobalCompliancePanel
This webinar will examine the existing and proposed requirements for the FDA's DHF -- including its derivative documents, the DMR and DHR.
Wednesday, November 2, 2011
10: 00 AM PDT | 01: 00 PM EDT
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The Drug Development Process - From RD to Commercialization - Webinar By GlobalCompliancePanel
In today's fast-paced, highly regulated and risk-aversive environment, functional groups can no longer work in isolation, but must collaborate extensively to design, develop, manufacture, test, validate and commercialize new drugs. Successful commercialization depends on effective processes to bring both the drug supply manufacturing processes and controls as well as the associated data and
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Implementing a Quality Systems-Based Approach to GCP Compliance - Webinar By GlobalCompliancePanel
Ensuring GCP quality has often been approached from the perspective of reviewing as many documents as possible, looking for errors and following up on corrections or making "notes to file." In order to design, implement, and maintain GCP compliance in an effective manner, a Quality Systems Approach should be adopted.
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From ZaranTech.com
SAP BOBJ with BW integration Online Competency Development Training program
TRAINING DETAILS:
Course Duration: 65 hours Training + Case Studies
Training Materials: All attendees would receive
a Assignment after each module,
a Notes and study material for examples covered.
Training Format: This course is delivered as a highly interactive session, with extensive live examples. This course is delivered in Online using Web and Audio Conferencing.
Timing:
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From GlobalCompliancePanel
Verification vs Validation in Regulated Industries - webinars by gcp
Attend this webinar to understand the differences and benefits of verification and validation.
Learn about the risks and complications involved with the application of sound verification and validation principles.
more...
Design Planning and Conducting Effective Audits - Webinars by gcp
Internal quality system audits should be viewed as an improvement tool. Too often due they have a negative connotation and are viewed as a necessary evil. Effective audits can comply with the regulations and also be a source of improvement.
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Design Planning and Conducting Effective Audits by gcp
Internal quality system audits should be viewed as an improvement tool. Too often due they have a negative connotation and are viewed as a necessary evil. Effective audits can comply with the regulations and also be a source of improvement.
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Validating Radiation Sterilization for Medical Device Industries by gcp
Gamma and E-Beam radiation has used for sterilization of medical devices for over 50 years. Both methods are validated following the same principles and standards. This webinar will provide an overview of the requirements to validate medical devices for both Gamma and E-Beam sterilization.
Validation is based on the international standard ISO 11137-1: 2006 and ISO 11137-2: 2006. In this one
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Using Statistics in Compensation BY Train HR
This webinar will address the math behind pay program design and administration, from the design of pay structures through the analysis of pay survey data that enables practitioners to create and analyze pay ranges, pay survey data, individual and group pay rates, and other elements of a compensation program.
more...
Statistical Concepts of Process Validation BY GCP
The FDA QSR requires device manufacturers to validate processes when the manufacturer cannot "fully verify the output". The manufacturer must validate these processes with a "high degree of assurance".
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Device Master Record Device History Record BY GCP
The FDA's Quality System Regulation (QSR) requires each device manufacturer to compile the specifications and procedures for a medical device.
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This Webinar will provide a substantive overview and outline differences between the Technical File and Design Dossier for those
This Webinar will provide a substantive overview and outline differences between the Technical File and Design Dossier for those device firms dealing with the global regulatory landscape.
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Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine
This webinar will provide valuable assistance to all device manufacturers, those who market solely within the US, or those who wish to market in the EU as well
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Pharmaceutical and Biologics Facility Design FDA and Regulatory Aspects by gcp
This course explores some of the best practices of pharmaceutical facility design with an emphasis on the regulatory aspect.
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The Controls for Outsourcing Manufacturing and Testing - Webinar By GlobalCompliancePanel
The Controls for Outsourcing Manufacturing and Testing" explores the use of outsourcing and how it impacts quality and compliance and the organization as a whole. The primary stakeholders and outsourcing include Quality, Research, Production, Laboratories, Purchasing/ Procurement, Finance, and Senior Management.
This webinar will study the outsourcing lifecycle and its impact on the
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How to Create Configure and Manage a Design Inputs - Design Outputs Traceability Matrix utilizing the principles of Lean Documen
Design Inputs, Design Outputs, and Traceability matrices present a challenge to almost all industries that apply design controls.
Typically, these cause the creation and maintenance of duplicate information across various documents - a major source of errors. This webinar applies the Theory of Lean Documents and the corresponding Theory of Lean Configuration to avoiding these errors, while
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Creation and management of a Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean
Controlled documents are one of the foundational building blocks of a Quality Management System (QMS) for regulated industries.
Too often, controlled documents are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed. This webinar applies the Theory of Lean Documents and the corresponding Theory of Lean Configuration to this key part of a QMS.
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Creation of DHFs DMRs and DHRs utilizing the principles of Lean Documents and Lean Configuration by GlobalCompliancePanel
Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR) are key building blocks used in the design, development, manufacturing, and cGMP compliance for the Medical Device Industry.
Too often, these are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed. This webinar applies the Theory of Lean Documents and also
more...
Creation of DHFs DMRs and DHRs utilizing the principles of Lean Documents and Lean Configuration - by GlobalCompliancePanel
Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR) are key building blocks used in the design, development, manufacturing, and cGMP compliance for the Medical Device Industry.
Too often, these are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed. This webinar applies the Theory of Lean Documents and also
more...
Master Production Record Requirements - Webinar By GlobalCompliancePanel
This program will address the 21CFR and Eudralex Volume 4 requirements and interpretation, as well as FDA Guidance regarding the creation, review and approval, and control of Master Production Records.
The material will enable attendees to establish a consistent approach to the design of MPR, including cover page content, instructions, processing requirements and limits, and signature
more...
Water System Design Start-Up and Validation - Webinar By GlobalCompliancePanel
This webinar provides a thorough examination of water systems. We will explore the typical components used in water systems and how these components are combined to achieve intended water quality specifications
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DHF DMR DHR Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel
Overview: This webinar will examine the existing and proposed requirements for the FDA's DHF - including its derivative documents, the DMR and DHR.
It will consider the MDD's TF/ DD requirements, and evaluate the documents' differing purposes / goals. Required and desirable contents will be discussed. Also considered: Areas requiring frequent re-evaluation / update; Similarities and
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Pharmaceutical and Medical Device Validation Guidances - Similarities and Differences - Webinar By GlobalCompliancePanel
Overview: This webinar will provide an overview of process validation for devices and pharmaceuticals.
While most of the webinar will include FDA compliance requirements, there will be some International Standards Organization (ISO), European, and Canadian regulations included for exploration. After attending this webinar, attendees will have a greater perspective of process validation and its
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Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel
Overview: CAPA is the most audited Quality subsystem in any Quality system. Most of the warning letters written by the FDA in 2010 were CAPA relate. Avoiding FDA CAPA findings starts with the design of a robust CAPA SYSTEM.
The webinar covers "Off-label statute" and the FDA's nonbinding off-label guidance as relates to re-prints, performance claims, and Promotion. Emphasis is placed on ethical,
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Develop and Execute the Company Software VV Program - Webinar By GlobalCompliancePanel
Overview: The verification and validation of medical software is coming under increased scrutiny by the U. S. FDA.
This webinar will address the use of the FDA, GAMP, 21 CFR Part 11, "Electronic Records" / "Electronic Signatures", and other applicable industry software validation models, coupled with the ISO 14971 / ICH Q9 Product Risk Management models, to structure, run, and document
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Recalls Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel
Overview: This webinar will acquaint one with the lessons learned from over 30 years of adverse events and complaints.
FDA has issued warning letters for failing to properly evaluate medical device complaints for reporting under 803 & 806 regulations. Vigilance reporting is also required in Canada, the European Union and many other countries. Warning letters and recalls are posted on FDA's
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FMEA and Risk Management for Medical Devices - Webinar By GlobalCompliancePanel
Overview: This presentation will explain the various terms used in risk management and the importance of ISO 14971 & ISO 13485 in the managements of risks during the life cycle of medical devices starting with design and manufacture.
FMEA (Failure Mode & Effects Analysis) is only a segment of Risk Management, but quite valuable for assessing Risk as part of Risk Management. Now that EN 1441
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Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine
Overview: This Webinar is designed for people involved in document preparation and maintenance, and those who have involvement with documentation.
The FDA QSR and the Medical Device Directive specify certain documents or records that should be included in your organization's quality systems - Design History File (DHF), the Device Master Record (DMR) the Device History Record (DHR), and the
more...
Conducting Successful Product Complaint Investigations - Webinar By GlobalCompliancePanel
Overview: This webinar will provide valuable assistance and guidance to the life sciences manufacturers engaged in various aspects of product complaint investigations.
An effective complaint handling system is an extremely important part of any quality system. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated
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The Most Common Problems in FDA Software Validation Verification- Webinar By GlobalCompliancePanel
Overview: This webinar will give valuable help to FDA regulated Pharmaceutical, Medical Device, Biotech, Diagnostics and Biological manufacturers.
In August 2010, FDA made an announcement affecting virtually every drug, device and biologic firm marketing products in the U. S:
"The Agency (FDA) will be conducting a series of inspections in an effort to evaluate industry's compliance and
more...
Understanding Attribute Acceptance Sampling including Z14 and c0 Plans -- Webinar By GlobalCompliancePanel
Overview: This course provides the attendees with the tools needed to understand and implement acceptance sampling.
We explain the basis for sampling plans, the binomial distribution, and show how it helps us understand the sampling plan's performance using the operating characteristic (OC) curve. Participants will gain a solid understanding of how the OC curve is built, how to use it, and how
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Requirements of the Master Production Record - Webinar By GlobalCompliancePanel
Overview: This program will address the 21CFR and Eudralex Volume 4 requirements and interpretation, as well as FDA Guidance regarding the creation, review and approval, and control of Master Production Records.
The material will enable attendees to establish a consistent approach to the design of MPR, including cover page content, instructions, processing requirements and limits, and signature
more...
Facilities Cleaning in Cleanrooms and Controlled Environments - Webinar By GlobalCompliancePanel
Overview: This live webinar concentrates on proper cleanroom cleaning, and discusses tools, equipment, agents, personnel training, extent, and frequencies.
It is a very practical training session intended to assist personnel involved in the design, cleaning, monitoring, and assessment of cleanroom cleaning procedures. The key benefits of this course are:
* In-dept understanding of
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Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel
Overview: Laboratory equipment should be calibrated and/ or qualified to demonstrate suitability for the intended use.
Laboratory systems including equipment are amongst key targets of FDA inspections. They are considered high risk systems because they have a high impact on product quality. Despite the fact that equipment calibration and qualification is nothing new and companies spend a lot of
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The Use and Mis-use of FMEA in Medical Device Risk Management - Webinar By GlobalCompliancePanel
Overview: The purpose of FMEA is to affect the design and the most practical time to do this is when competing designs are being considered, not after choices have been made, contracts signed, and prototypes being built and tested.
Of course, there are other reasons for performing a FMEA. FDA requires risk assessment (hazard analysis) but a FMEA conducted late in the product development process
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Understanding ISO 13485 vs ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel
Overview: ISO 13485: 2003 is a quality management system standard specially written for the medical device industry and is on the U S Food & Drug Administration (FDA) list of recognized consensus standards.
Medical device firms certified to ISO 13485: 2003 will find themselves very closely compliant with FDA's Quality System Requirements under 21CFR 820. This presentation will help you to
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The Pharmaceutical Quality System - Webinar By GlobalCompliancePanel
Overview: This webinar will discuss the evolution of the standards, describe a Pharmaceutical Quality System and discuss the transition to the Pharmaceutical Quality System.
Why you should attend: The US FDA, and regulatory agencies around the world, are actively promoting the concept of a Pharmaceutical Quality System. The concept of a Quality System was imposed on the medical device industry
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A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - W
Overview: As a quality professional, you desire to have the very best quality system that operates effectively, efficiently and conforms to the appropriate quality standards to meet customer and user needs.
You are also aware that there is a paradigm shift from an emphasis on compliance to an emphasis on quality based systems. An understanding of this paradigm shift can be gained by comparing
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Bringing Compliance To Design Control For Older Products - Webinar By GlobalCompliancePanel
Overview: The webinar examines critical parts of design control after product release including: design change control, design validation, and the Design History File.
The webinar is designed to help regulatory Affairs, Quality Engineers, and Design Engineers maintain released products within current regulatory requirements. As an attendee you will learn what the FDAs expectations for your
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Documentation for IEC 60601-1 3rd Edition Compliance - Webinar By GlobalCompliancePanel
Overview: In this presentation we will review the certification requirements for documentation of the clauses of IEC 60601-1 Third Edition.
The purpose will be to provide medical device manufacturers with information on how to provide certification bodies with the information they need to certify products to the Third Edition in the most efficient manner. By preparing in advance for
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Developing the Risk Management Plan - Webinar By GlobalCompliancePanel
Overview: This presentation will review the requirements for the Risk Management Plan and discuss practical methods for meeting the requirements.
Examples of documentation of the Plan will be presented, including Risk Acceptability Criteria, risk review, verification activities, and information collection activities. While Risk Management Plans can be part of the Quality Plans for a product,
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Validating Rapid Microbiological Methods - Webinar By GlobalCompliancePanel
Overview: Method validation is the process used to confirm that an analytical procedure employed for a specific test is reliable, reproducible and suitable for its intended purpose.
All analytical methods need to be validated prior to their introduction into routine use, and this is especially true for novel technology platforms, such as rapid microbiological methods (RMMs).
Because many RMM
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Design Control for Medical Devices - Webinar By GlobalCompliancePanel
Overview: Prior to introduction of a new device, or even a modified design for an existing device, a systematic process must be followed.
This process must ensure that all requirements are met. A firm's design control process must meet all regulatory requirements, but at the same time not be so unwieldy as the present a barrier to timely market introduction.
This webinar will cover the
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Process Validation for Medical Devices - Webinar By GlobalCompliancePanel
Overview: This course provides regulatory/ quality professionals, manufacturing engineers, and process development engineers with the knowledge and skills needed to comply with the process validation requirements of the FDA's Quality System Regulation, ISO 13485 and the GHTF Validation guidance N99-10 while offering information on how to implement an effective validation program.
The purpose of
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Project Management for Clinical Trials - Webinar By GlobalCompliancePanel
Overview: This web seminar has been designed to provide you with a clear understanding of project management skills to apply to running clinical trials.
It will ensure you gain a clear understanding of the tools and techniques of project management for clinical trial and how they can be applied to your own pharmaceutical projects in the work place. In addition to key project management tools
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Developing and Using the Product Risk Management FileReport - Webinar By GlobalCompliancePanel
Overview: Expectations for meaningful hazard analysis, hazardous conditions, and documentation have always existed by regulatory agencies.
There is an increased awareness of the importance of design activities to support the production of safe and effective product. Product risk management is a required tool to drive and direct resource constrained product design, manufacture and validation
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Change Control -- Your Companys GMP Weak Point - Webinar By GlobalCompliancePanel
Overview: There is a pervasive public perception that the FDA has been ineffective in protecting the public.
Recent news events in foods, drugs, and devices seem to support this perception. The "tougher" FDA is determined to change that perception. Industry must be prepared to adapt, and recognize that such adaptation will actually work to their long-term benefit. This webinar will discuss and
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From Guru - Your Online Mentor
Asterisk telephony Infrastructure setup




Design & build telephony infrastructure using Asterisk.
Agenda:
1. Introduction to Telephony
2. Understanding IP telephony
3. Understanding traditional PBX and Soft PBX.
4. Overview to Asterisk & related products.
5. Installing AsteriskNOW
6. Installing Elastix
7. Adding basic components - extensions, trunk, outboundroute etc.,
8. Working with Ring groups, VoiceMail & IVR.
9.
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From GlobalCompliancePanel
Excel Spreadsheets and FDA Device Regulations - Webinar by GlobalCompliancePanel
Overview: This webinar helps you understand the FDA device regulations related to Excel spreadsheets.
These spreadsheets can be automated processes and create electronic records. Both of these aspects are regulated by the FDA, so device manufacturers must understand the regulations and how to apply them. The seminar begins with Excel methods to help ensure the spreadsheet produces the results
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Cleanroom HEPA Filter Testing Certification An Owners Guide - Webinar by GlobalCompliancePanel
Overview: This webinar concentrates on identifying and discussing testing and certification requirements associated with cleanrooms.
The key benefits of this course are:
* In-dept understanding of industry standards, processes, and criteria for testing cleanrooms and HEPA filters
* Achieve satisfactory inspections more easily
* Higher assurance of new medical product approvals
more...
Reprocessing REUSABLE Medical Devices-Cleaning Labeling Requirements - Webinar By GlobalCompliancePanel
Overview: Much attention has been paid to the regulatory requirements of reprocessing SINGLE use devices.
However, there is increasing attention being directed towards reprocessing REUSABLE medical devices and regulatory requirements. The purpose of this seminar is to explain the rationale, the legal requirements and some methods commonly used for reprocessing & validating reusable medical
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Food Safety Management Systems - ISO 220002005 - Webinar By GlobalCompliancePanel
Overview: This presentation will assist organizations within the food chain to understand the requirements to meet the international standard for Food Safety Management.
Areas Covered in the Session: The following areas will be addressed:
* Key terms and definitions
* General Requirements
* Documentation
* Management Responsibility
* Resource Management
*
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Hazard Analysis vs FMECA Differences and Commonalities - Webinar By GlobalCompliancePanel
Overview: The terms "Hazard and Risk Analysis" and "Failure Mode, Effects and Criticality Analysis (FMECA)" are often used synonymously.
However, there are significant differences in both methodologies and their strengths can be combined to ensure a safe and efficacious system design. The presentation will explain both methodologies and will show ways how these tools can be used to complement
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Labeling Requirements for Dietary Supplements - Webinar By GlobalCompliancePanel
Overview: This webinar points out current labeling issues including misbranding that are eating into profitability of dietary companies.
The webinar teaches the attendee how to avoid common labeling compliance issues including:
* Misbranding
* Misleading claims
* Misleading statements
* Directions of use
The webinar focuses on general labeling provisions for dietary
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Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel
Overview: This webinar will provide valuable guidance to regulated companies in development and implementation of Project Management Planning and Techniques for new product development, regulatory compliance audit responses, proof of "progress against plan", and other activities requiring a planned documented rationale.
Three of the most common tools will be discussed. One very simple approach
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Effective Training Practices for FDA Compliance - Webinar By GlobalCompliancePanel
Overview: This presentation will answer some of the frequent questions of new trainers or training managers. These include: worker training requirements, the frequency of training, how do design an effective training program, who is responsible for training, training effectives and training documentation.
By examining the GMP expectations on training from different regulatory bodies (from the
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Using Foreign Trial Data in Your NDA Approval Process - Webinar By GlobalCompliancePanel
Overview: In this NDA Approval Process training Webinar learn the guidance and regulations governing FDAa s acceptance of foreign trial data and know how FDA implementing these rule along with design considerations and requirements for foreign trials.
Why you should attend: While the law allows 100 percent of pivotal data to come from foreign trials, there have been very few such
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Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel
Overview: It is an unfortunate fact that most water systems today have been designed and are operated and controlled using at least some traditional concepts and methods that are downright wrong.
So how could such traditions become so ingrained and be so wrong? How could well-intentioned benchmarking be so misguided? There are many reasons, which will be discussed, but regardless of the causes,
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Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel
Overview: The FDA generally defines combination products as a product composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device, and a biological product.
Although there are differences between these quality systems, the quality principles embodied in the systems are the same. This course looks at these principles
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How to Prepare and Submit a Bullet Proof 510k and Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanel
Overview: This 3 hour Webinar is a primer and overview to the premarket notification process, i. e., a 510(k).
A 510(k) is a premarket submission made to FDA to demonstrate that your device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device that is not subject to PMA. There are three types of Premarket Notification 510(k)s that may
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Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine
Overview: The FDA QSR and the Medical Device Directive specify certain documents or records that should be included in your organization's quality systems - Design History File (DHF), the Device Master Record (DMR) the Device History Record (DHR), and the Technical File (TF).
Do you know what information should reside in a DHF, a DMR and a DHR? This Webinar will define, explain and clarify the
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Key Concepts in Successful Water System Sanitization - Webinar By GlobalCompliancePanel
Overview: Though hardly a water system is designed and installed without some capability of sanitization, the system design features, materials of construction, sanitization approach, as well as the frequency of the sanitization process have everything to do with its success.
This presentation focuses on the factors that can lead to water system sanitization success as well as failure so that
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The Process Approach to Auditing - Webinar By GlobalCompliancepanel
Overview: The structure of ISO 9001: 2000 provides a focus on the processes that comprise the quality management system (QMS). Also, the general requirements laid out in Clause 4. 1, the foundation for auditing a process-based system, are taken up for discussion at this webinar.
There are eight basic processes that an organization must have to function effectively. These are:
*
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Construct and Manage the Technical File and Design Dossier - Webinar By GlobalCompliancePanel
Overview: This Webinar will provide a substantive overview and outline differences between the Technical File and Design Dossier for those device firms dealing with the global regulatory landscape. It is assumed that participants and customers have a prior CE Mark and Medical Device Directive background.
The Technical File is a comprehensive collection of information and documents that details
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The Drug Development Path - From RD to Commercialization - Webinar By GlobalCompliancePanel
An overview of the drug development process, reviewing key deliverables for each stage of the development path with a special focus on managing the development process when using external resources such as Contract Manufactures, Contract Testing Labs and Contract Research Organizations.
In today's fast-paced, highly regulated and risk-aversive environment, functional groups can no longer work
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Full Day Virtual Seminar - Designing and Implementing the Quality System for Combination Products - by GlobalCompliancePanel
The FDA generally defines combination products as a product composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device, and a biological product.
Although there are differences between these quality systems, the quality principles embodied in the systems are the same. This course looks at these principles and the
more...
Interfacing Design Verification Process Validation and Design Validation - Webinar by GlobalCompliancePanel
There is confusion between the requirements for Design Verification, Process Validation and Design Validation.
While each of these processes has its own requirements, they do not stand alone, they are linked together. As this linkage is not well understood, it is the source of FDA observations and potential release of products that do not meet requirements.
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The Most Common Problems in FDA Software Validation Verification - Webinar by GlobalCompliancePanel
In August 2010, FDA made an announcement affecting virtually every drug, device and biologic firm marketing products in the U. S:
"The Agency (FDA) will be conducting a series of inspections in an effort to evaluate industry's compliance and understanding of Part 11...The Agency intends to take appropriate action to enforce Part 11 requirements for issues raised during the inspections..."
more...
Revamping the 510k Clearance Process-Understanding FDAs Proposals - Webinar by GlobalCompliancePanel
The FDA has proposed an overhaul of the 510(k) clearance system In its release of reports from two working groups, the FDA's goals are to increase the predictability and transparency of the 510(k) process and enhance FDA scientific decision-making.
It will also increase the burdens on industry. For example, if finalized, there will be a new subclass of Class 2 products for which clinical
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Statistical Concepts of Process Validation - Webinar by GlobalCompliancePanel
The FDA QSR requires device manufacturers to validate processes when the manufacturer cannot "fully verify the output".
The manufacturer must validate these processes with a "high degree of assurance". The presentation explores the statistical underpinnings of these two phrases. To "fully verify the output" relates to the use of statistical sampling plans, while "high degree of precision"
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Navigating Pediatric Trials from recruitment to successful on-time completion - Webinar by GlobalCompliancePanel
Drug companies face many challenges in pediatric clinical research. Pediatric trials come with a high level of complexity and cost.
In order for professionals to carry out a successful pediatric drug development plan, they need the right infrastructure and information to avoid obstacles such as slow recruitment, noncompliance and difficulties in developing the right study criteria and protocol.
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Managing the IDE Investigational Device Exemption Submission for Compliance Success - Webinar by GlobalCompliancePanel
An investigational device exemption (IDE) allows the investigational device to be used in a clinical study in order to collect safety and effectiveness data required to support a Premarket Approval (PMA) application or a Premarket Notification [510(k)] submission to FDA.
Clinical studies are most often conducted to support a PMA. Only a small percentage of 510(k)'s require clinical data to
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Robust Process Validation for Medical Devices - Webinar by GlobalCompliancePanel
One of the most common reasons noted by the FDA for recalls of medical device is improper validation.
It is also one of the most common reasons companies receive 483s and warning letters. Conversely, successful validations not only satisfy compliance and regulatory requirements, they also provide for robust manufacturing processes satisfying the needs of many individual functions within your
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The DHF Technical File and Design Dossier - Similarities Differences and The Future - Webinar by GlobalCompliancePanel
This webinar will examine the existing and proposed requiements for the FDA's DHF and the MDD's TF/ DD. Differing purposes / goals. Differing purposes / goals. Required and desirable contents. Areas requiring frequent re-evaluation / update. Similiarities and differences, and future trends. Typical DHF Table of Contents. Technical File or Design Dossier Table of Contents. The importance and
more...
Important Sterilization Information for Product Developers - Webinar by GlobalCompliancePanel
Product developers have the responsibility of the development of medical devices or healthcare products that will be sterilized; however they may not have an adequate understanding of the sterilization processes and its impact to the functionality of the product and its package. This presentation will provide information that can be used by R&D Engineers and Product Developers to aid them in the
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From NEi Software
Advancements in Simulation Series Webinar 4 Analysis Optimization

Webinar 4: Analysis Optimization
Register for this series of complimentary webinars to learn about advancements in software driven product design testing. Engineers will gain insight into how to use the latest FEA software innovations to help meet business objectives such as reducing material costs, time to market and field failures.
NEi Software FEA experts will provide specific
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Advancements in Simulation Series Webinar 3 Nonlinear Analysis

Webinar 3: Nonlinear Analysis
Register for this series of complimentary webinars to learn about advancements in software driven product design testing. Engineers will gain insight into how to use the latest FEA software innovations to help meet business objectives such as reducing material costs, time to market and field failures.
NEi Software FEA experts will provide specific
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From XA Systems
ITIL Foundation Bridge Virtual Classroom
Take the ITIL ® v3 Foundation Bridge course Virtual Classroom is set up in the same manner as the physical classroom however altered to optimize the virtual learning experience without the hassle of travel. The virtual classroom delivery option is ideal for training geographically dispersed teams.
This 2-day course introduces learners to the lifecycle of managing IT services to deliver to
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ITIL v3 Foundation Virtual Classroom
Take the ITIL ® v3 Foundation course Virtual Classroom is set up in the same manner as the physical classroom however altered to optimize the virtual learning experience without the hassle of travel. The virtual classroom delivery option is ideal for training geographically dispersed teams.
This exciting and dynamic 3-day course introduces learners to the lifecycle of managing IT services
more...
From GlobalCompliancePanel
Design Planning and conducting Effective audits
GlobalCompliancePanel brings a new webinar on the topic of Design, Planning and conducting Effective audits.
Webinar will be on March 23, 2010. Webinar will be presented by Mark Roberts.
Internal quality system audits should be viewed as an improvement tool. Too often due they have a negative connotation and are viewed as a necessary evil. Effective audits can comply with the regulations and
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From Performance Systems Development
Online Building Science Series March - August 2010
If you are interested in learning about the fundamentals of building science and the energy efficiency industry, or becoming a certified Energy Auditor, this series of online courses is for you. Every other week starting in March 2010, our online series will support you in becoming a building performance professional from the comfort of your home or office. Each interactive course is presented in
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From University of Kansas Continuing Education
Maintenance Management Online Certificate Course

The Online Certificate Program in Maintenance Management consists of three modules, which will help you evaluate your operation; plan, coordinate and schedule maintenance; and properly use preventive and predictive maintenance in your operation. The program is designed for all types of maintenance environments including refineries, chemical plants, factories, mines, large buildings, organizations
more...
Process Instrumentation and Control Online Certificate Course
The online certificate program in Process Instrumentation and Control (I&C) consists of three modules covering the different phases of I&C from a nonmathematical and practical point of view. It includes basic concepts, engineering, and installation of control equipment.
The attendees will learn about:
1. Basics of I&C, including different control functions, types of control loops, and
more...
From Strategic Agile Technologies
Complete Java Training
Complete Java & J2EE Online Training Course Details
* Duration: 3 to 3. 5 months
* Timing: Every alternate day in week day and both week ends.
* This course is Free for new students for first 2 weeks.
* Pricing: 990$ (Including taxes) (Saves you 300$).
* We beet all our competitors prices.
* Register now
Complete Java & J2EE Training Course Details
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From Design By DesAnn
Home Staging Summer School Webinar Series



What: Staging Summer School Webinar Series
When: August 9 and 16th, 7-8: 30 PM or access to recording
Where: Online Webinar
Who: The Decorating and Staging Academy does it again!
Cost: $118 for 2 webinars and follow up home assignment for assessment
Do you want to gear up for Fall with new and creative ideas to make the most from your Staging Business? Or maybe you simply want more
more...
From Rescue Institute
Executive Coach Training- Just 179 SHRM and CPD Approved




Do youa
Think you could be a good Executive Coach (internal or external)?
Want to find out for sure before you spend a ton of money on training?
Need to hear the real truth about Executive Coaching from a former Fortune 100 executive and one of the top Executive Coaches?
Are you interested in Executive Coaching?
more...
From Fire Tech Productions, Inc
NICET Water Based System Layout Level I CBT Webinar Series





This Level I NICET Water-Based Systems Layout webinar series is the best exam prep around! Learn the information, tips and techniques needed to pass the exam from Industry Leaders with over 50 years experience. This package contains 2 1. 5 hour LIVE sessions, online course access for 90 days, recorded versions of each session and our Level I Basic Water Based Systems Layout Reference Text.
more...
From GC Learning Services LLC
Customer Service Skills





The goals to be accomplished in this course are to:
a Recognize the characteristics of proper telephone and voicemail etiquette.
a Identify ways to use good communication skills both verbal and non-verbal, to address customer concerns and uncover needs.
a Identify various sales and customer service techniques to up sell and cross sell as appropriate
more...
From Parameter Security
ECSA Certified Security Analyst
Plan & Design Networks
Implement Security Solutions
Analyze Security Risks & Threats
Why Get E|CSA Certified?
EC-Council Certified Security Analyst (E|CSA) complements the Certified Ethical Hacker (C|EH) certification by exploring the analytical phase of ethical hacking. While C|EH exposes the learner to hacking tools and technologies, E|CSA takes it a step further by exploring how to
more...
Licensed Penetration Tester Certified Security Analyst - ECSALPT
You're C|EH Certified. Now What?
Become a Licensed Penetration Tester.
Take It to the Next Level.
Become a Certified Security Analyst / Licensed Penetration Tester.
ECSA/ LPT
(All from the comfort of your home or office.)
September 13 - 17, 2010
Advanced Hacking, Penetration Testing & Security Analysis
EC-Council Certified Security Analyst (ECSA) complements the Certified Ethical
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From Consepsys Oil and Gas
Waxy Crude - What Every Oil and Gas Professional Should Know
This course aims at dramatically improving the understanding of waxy crude amongst Oil and Gas professionals. It focuses on little known aspects of waxy crude behaviour, which, when they are ignored, cost significant amounts of money to Oil and Gas operators in production downtime, cleaning campaigns, mitigation through chemical treatment, off-specification product penalties, wax-related
more...
From International Contact Center Academy
Contact Center Staff Engagement Wellness Webinar


Work-life balance is an indicator of health. Yet it seems that almost everyone has too much to do and not enough time to do it. Many things are constantly competing for your time and energy. Contact Centers today who want to attract and keep their talented workers understand the connection between employee satisfaction and employee wellness. They believe that workplace wellness is a business
more...
From Business901
Marketing Your Black Belt
Marketing Your Black Belt
How Good are you at Marketing Yourself?
Presentation on "How to Market Black Belt Services!"
All Attendees will receive a Free download of
How to Achieve Expert Status in 2010
Cana t make this time, please contact us for other available times.
I believe that Lean Six Sigma Consulting has the greatest opportunity ever and in my terms,
more...
From CSS Computer Education
Computer Education Franchisee registered study center
CSS (College of Software Society) Computer Education has built a reputation as a global provider for quality computer education.
CSS offers a wide range of long-term and short-term IT courses. CSS has long established itself as a global learning solutions provider, High-end IT Training & Induction Training for Software Developers.
Our strong research orientation has helped us continuously
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From iGallant Solutions
ITIL V3 Foundation
ITIL V3 Foundation (Online / Classroom Training)
Overview
ITIL ® is recognized best practices for IT Service Management field and It has five life cycle phases and Capability Modules.
The purpose of the ITIL ® Foundation certificate in IT Service Management is to obtain knowledge of the ITIL ® terminology, structure and basic concepts and to comprehend the core principles of ITIL
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From Olympus Training Ltd
Level 3 Certificate in Personal Training
Level 3 Certificate in Personal Training.
The aim of this qualification is to recognise the skills, knowledge and competence required for an individual to work unsupervised as a personal trainer. This includes being able to offer one-to-one training, baseline assessment, nutritional advice and progressive programming which is specific to the individual needs of a client.
Level 3 Personal
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Level 2 Gym Instructor courses
In many ways this is one of the landmark courses we deliver. This is because on completion it qualifies the candidate to work in a fitness suite as a gym instructor. It also allows people to move onto other specialisma s such as personal training and/ or class teaching. We deliver courses in Ipswich, Norwich, London, Liverpool, and Thetford.
Level 2 Gym Instructor Courses cover:
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From 4MAT 4Business
4MAT Instructional Design Online Certification
Join us May 18-July for this 6 part series now!
*Register now and receive 1-year subscription to the 4MATion ® Online Training Design Center ($299 Value) to create, store and assess your designs online!
All classes are held between 10: 30 am-12 pm Central.
This is not a theory-based, all-talk webinar. Youa ll experience 4MAT ® as you learn about 4MAT ®. Our web-based
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Free Online Course 4MAT 8-Steps to Design
The Secret to Learning: The Four Questions That Must Be Answered
The secret to engaging instructional design and delivery: all learning includes the asking and answering of four questions. These questions form a cycle of learning. This four-part cycle applies to learning anything. You followed this cycle when you learned to ride a bike, when you learned that second language in high school and
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Inform 10 Activity Frameworks for Increasing Interactivity in Lecture
Who should attend: Instructional Designers and Trainers
In Step 4, Inform, the trainer shares the information the learner must know to generate the desired learning outcomes. This is typically where the trainer lectures. However, lecture isna t all talk. How do we make lecture interactive and engaging? In this session, we will explore 10 structures for increasing interactivity. Structures
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Too Much Information Too Little Time How to Conceptualize Content
Who should attend: Instructional Designers
When: April 19, 2011 at 2 pm Central
You are tasked with sharing an enormous amount of information in a short period of time. In this session, we will explore strategies for increasing retention and engagement. You will explore how to define a concept for your courses and practice conceptualizing content using movies and real-world content.
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Trainers Toolkit Inventory of Training Tools and Techniques for Dynamic Delivery in all Four Parts of the Learning Cycle
Who should attend: Instructional Designers and Trainers
There are four parts to the 4MAT Learning Cycle: Engage, Share, Practice and Perform. In this session, you will explore easy-to-apply concrete tools and techniques for guiding the learning process. Youa ll see examples of how these tools can be used in live and online training with any content.
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From Scientiabio
Online LIVE training in Bioinformatics and Clinical Research




ScientiaBio Team brings an unique opportunity for basic and advanced level Bioinformatics training online.
The topic that we generally cover is mentioned below :
1. Basic Bioinformatics
2. Protein Structure Determination and Protein Modeling
3. I silico Drug Designing
4. In silico ADME and Toxicity Analysis
5. Basics of Microarray and MIcroarray Data Analysis
6. Systems Biology
7.
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From InfoStar International
PeopleSoft PeopleTools Upgrade and Data Management Rel 850
InfoStar International Leader in Oracle and PeopleSoft Consulting, Implementations, Upgrades, Production support and Training center offers the following course in class room. On-site corporate training and Instructor Lead-Online training.
Course Duration: 40 hours
Full-time: 1 week
Weekend: 2-3 Weekends
Part-time: 8-10 hours per week
Flexible schedule!!
PeopleSoft PeopleTools Upgrade
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From TSN Technology
6 Months Industrial Training in Delhi for B TechBEMCA
TSN Technology, a global IT solution company providing full-cycle services in areas of Software Development, web design and development, web application development, professional ecommerce online shopping systems, Flash multimedia, website hosting, search engine promotion (SEO), portal development and graphics design. Combining our solid business domain experience, technical expertise, profound
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From Pioneer Engineering
Resonance in regard to Vibration



Resonance
Synopsis
Resonance is one of the most common, and likely the most damaging vibration problem in industry today.
Expand your vibration analysis "toolbox" by adding resonance analysis to it. Learn the proper signal processing settings, the applications, limitations, analysis techniques, and resources required in order to implement Resonance Analysis.
Learning Objectives:
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Proactive Maintenance Management




Proactive Maintenance Management
Synopsis Learn how to change from reactionary maintenance to
proactive maintenance. This course covers the fundamental strategies required to improve reliability.
Prerequisites: Minimum 6 months industrial plant experience
Course Length 8 Hours
Certification Exam 20 questions, 1 hours time limit, closed book but a summary sheet of formulae is
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Machine Theory AC and DC Motors

Machine Theory a AC and DC Motors
Synopsis
This course covers the machine theory as well as specific vibration analysis for
proper maintenance, trending, and analysis of AC and DC Motors. The course
starts with the theory of operation and design of AC and DC Motors. It then
moves on to vibration analysis techniques by establishing the appropriate
hardware & software selection and
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Machine Theory Bearings


Synopsis
This course covers the machine theory as well as specific vibration analysis for proper maintenance, trending, and analysis of rolling element and fluid film bearings. The course starts with the theory of operation and design of rolling element and fluid film bearings. It then moves on to vibration analysis techniques by establishing the appropriate hardware & software selection and
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Machine Theory Belts and Couplings



Machine Theory a Belts and Couplings
Synopsis
This course covers the machine theory as well as specific vibration analysis for
proper maintenance, trending, and analysis of belts and couplings. The course
starts with the theory of operation and design of belts and couplings. It then
moves on to vibration analysis techniques by establishing the appropriate
hardware & software
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Machine Theory Centrifugal Pumps Fans and Compressors


Machine Theory a Centrifugal Pumps, Fans, and Compressors
Synopsis
This course covers the machine theory as well as specific vibration analysis for
proper maintenance, trending, and analysis of centrifugal pumps, fans, and
compressors. The course starts with the theory of operation and design of
pumps, fans, and compressors. It then moves on to vibration analysis
techniques by
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Machine Theory Gears

Machine Theory a Gears
Synopsis
This course covers the machine theory as well as specific vibration analysis for
proper maintenance, trending, and analysis of gears. The course starts with the
theory of operation and design of gears. It then moves on to vibration analysis
techniques by establishing the appropriate hardware & software selection and
setup for trending and diagnosis.
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From Staging and Redesign
Curb Appeal Confidence Course for Staging and Redesign with Michelle Molinari of CurbAppealForDummiescom
Curb Appeal Confidence Course for Staging and Redesign with Michelle Molinari of CurbAppealForDummies. com
Join us for a Webinar on September 15
Space is limited.
Reserve your Webinar seat now at:
https://www1. gotomeeting. com/ register/ 893470273
Michelle Molinari is the owner of CurbAppealforDummies. com, and has been dubbed 'The Queen of Curb Appeal" by her clients and
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From Keen Info Solution
SAP ABAP Online Training ECC 60
Course Content of SAP ABAP Module
1 Introduction to SAP
* Introduction to ERP
* Overview of SAP
* SAP modules at a Glance
2 Landscape & SAP R/ 3 Architecture
* Landscape Model
* Overview of R/ 3
3 ABAP Data Types
* Character
* Integer
* Numeric Character
* Floating Point
* Packed Decimals
* Time
* Date,
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Oracle Financial R12 Online Training
ORACLE FINANCIALS
Course: Oracle Finance Duration: 30 w. days Classes: 2 hrs
a Introduction to ERP
o Introduction
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From Compucount Business Services, Inc.
Peachtree Software - Financial Statements
Covers Financial Statement design using the Design Wizard.
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From Keen Info Solution
Online Training for SAP ABAP ECC 60 with 6y Real Time Expert
AP - ABAP ECC 6. 0
Course Content :-
1 Introduction to SAP
* Introduction to ERP
* Overview of SAP
* SAP modules at a Glance
2 Landscape & SAP R/ 3 Architecture
* Landscape Model
* Overview of R/ 3
3 ABAP Data Types
* Character
* Integer
* Numeric Character
* Floating Point
* Packed Decimals
* Time
* Date, Strings
4 Loops & Branches
* Do, Do n times,
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Online Training for Microsoft BI with 6 years Real Time Expert
SSIS (Total 35Hours)
Module 1:
Introduction to SQL Server 2005
Integration Services
This module introduces the role that Integration Services plays in extracting,
transforming, and loading data. This module also describes the tools that you can use to
build and manage Integration Services solutions.
a Overview of Integration Services Solutions
a Integration Services Tools
Module 2:
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Online Training for Oracle RAC DBA with 6y Real Time Expert
Oracle a RAC
Course Contents:
Day 1:
Unit1
Introduction and installation
Advantage of using RAC
Architecture of RAC
Cache fusion,
Multi instance transaction behavior
Extra background process in RAC
Day 2:
Unit -2
Oracle RAC 10G installation
Pre-requisite before installation
Unit-3
Clusterware installation
ASM installation
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Online Training for Oracle Financial R12 with 6y Real Time Expert


ORACLE FINANCIALS
Introduction to ERP
o Introduction to ERP
o What is oracle
o History of Oracle & People behind Oracle Corp
o What is Oracle Application/ E-Business suite
o Versions available in Oracle
o Versions available in Oracle Application
o What are major modules available in Oracle Application
o ERPa s available in the market
o Why Oracle application
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From 4BS Solutions
webmethods 8 training


Mail: eai. architects@gmail. comwmtrainings@gmail. comAbout 4BS Solutions4BS Solutions is an Indian based fast growing Online Training company which offers World class training in webMethods, TIBCO, JCAPS, Websphere MQ/ MB &Other Technologies for everyone in the world (US, UK, AUS, UAE, Singaporea ) every week for your convenience time by a Real Time Professionals. WebMethodsTraining from Real
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From Business Expert Webinars
Advanced Customer Service Planning for Services Firms
Align Your Firm s Service Delivery With The Desires of Your Clients
According to the American Society of Quality, 68% of clients leave because of an attitude of indifference from a company employee. Excellent customer service doesn't happen by accident. It is designed, planned, and scripted to account for every aspect of the customer service experience. Most services firms cross their fingers
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Get New Sales People Generating Revenue Fast
Develop a Plan That Quickly Gets New Hires Up to Speed
As a sales manager, you rely entirely on your sales team for revenue performance; and succeed or fail based on how they do. Your ability to effectively onboard your newly- hired sales people will make or break your year. Every moment that your new sales person is not armed to sell translates to lost sales opportunities and is a glaring cost
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How to Become A Great Sales Leader
Learn The Secrets to Building A Winning Sales Team
Baseball managers don't throw a pitch or hit a ball. They lead their team through thick and thin to deliver victories. As a sales manager, you rely on your sales team to hit homeruns every day. In a challenged economy, your sales team may be finding it tough to take a good swing at the plate these days. Your sales team is looking to you for
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How to Run Effective Internal Meetings
Increase Productivity with Well-Run Meetings
As you are searching high and low for the costs that are dooming your business, you are forgetting one of the most expensive ones unproductive, unnecessary meetings. Talk to your employees and you will hear the complaints fly: being invited to meetings that are not geared toward them meetings that are poorly run and meetings that were not needed at
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After the Handshake
Networking Strategies to Propel Your Business
'I shook a lot of hands at the event but now what? How do I turn the business cards I collected into real business relationships?' Networking is a powerful way to convert suspects into prospects if you do it correctly. Unfortunately, most professionals don t. Instead, you have dozens of tongue-tied conversations at industry events worrying whether you
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Get New Sales People Generating Revenue Fast
Develop a Plan That Quickly Gets New Hires Up to Speed
As a sales manager, you rely entirely on your sales team for revenue performance; and succeed or fail based on how they do. Your ability to effectively onboard your newly- hired sales people will make or break your year. Every moment that your new sales person is not armed to sell translates to lost sales opportunities and is a glaring cost
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How to Develop Your Employees with Little Investment
Improve performance through self-directed learning
Cuts hit the training budget hard. Yet, despite the economic crunch, employee development remains a critical requirement of a successful company. Resources are scarce, budgets are tight, but the companies that survive and thrive are those who learn the secrets to training their employees without breaking the bank.
Tim Hagen, salesforce
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Forecasting & Pipeline Management
How to Eliminate Stalled Opportunities from Your Company s Sales Opportunity Pipeline
What is the condition of your company s sales opportunity pipeline? How many of the opportunities have been stalled at the same step in the sales cycle for weeks or months?
If sales forecasts and opportunity pipelines are inaccurate, or if opportunities do not close in predictable time frames, it can wreak
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How to Grow Profits In a Recession
Strategies to Protect Your Bottom-Line
The economic squeeze has conditioned most business leaders to operate in reactive mode to ensure survival but this approach jeopardizes the future of the company. For your company to remain profitable now, and in the future, you need to become proactive so that you make prudent decisions not knee-jerk reactions.
John Myrna, author of '100 Quick Tips for
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Stop Running Your Business By the Seat of Your Pants
Design an Action Plan That Works for You
Having a strong foundation enables you to build a thriving, profitable life and business. Learn to be the architect of your own life and business.
Topics covered in this lively, interactive presentation are:
1. Discovery - To make sure you are on the right path, headed in the right direction and positioned properly.
2. Vision Determine clarity on
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Develop A Marketing Plan to Retain and Grow Your Customer Base
Uncover the Secrets About Your Customer's Buying Habits
You've heard it before. It's much more costly to find a new customer than to expand the buying relationship with an existing one. While the concept is not new or revolutionary, most companies don't know what drives their customers to buy, and what else they can sell them. Worse yet, they leave the door wide-open for their competitors to
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How to Become A Great Sales Leader
Learn The Secrets to Building A Winning Sales Team
Baseball managers don't throw a pitch or hit a ball. They lead their team through thick and thin to deliver victories. As a sales manager, you rely on your sales team to hit homeruns every day. In a challenged economy, your sales team may be finding it tough to take a good swing at the plate these days. Your sales team is looking to you for
more...
Stop Stifling the Growth of Your Company!
Learn how to remove the blinders that limit potential
As a business owner and entrepreneur, are you focused on the big picture of where your company needs to go or do you only see a tiny microcosm and fight for crumbs? The Achilles' heel of many executives is that they have a vivid image of the little picture, but pay little attention to the big vision. They lead companies that have little
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Get New Sales People Generating Revenue Fast
Develop a Plan That Quickly Gets New Hires Up to Speed
As a sales manager, you rely entirely on your sales team for revenue performance; and succeed or fail based on how they do. Your ability to effectively onboard your newly- hired sales people will make or break your year. Every moment that your new sales person is not armed to sell translates to lost sales opportunities and is a glaring cost
more...
Create a Sticky Lead Nurturing Process
Use e-marketing to increase qualified leads and shorten sales cycles.
According to Marketing Sherpa, 64% of companies with a lead nurturing process are dissatisfied with their results.
Every company needs more sales-ready leads. But, unless nurturing content syncs with the way they think, the dissatisfaction will continue. Your leads have taken control of the buying process. They decide when or
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Use Direct Mail Effectively On A Tight Budget
Secrets to Using This Forgotten, Yet Effective, Marketing Tool
Internet marketing is a glitzy marketing approach that has caused many marketing professionals to forget about tried-and-true direct mail marketing campaigns. While direct mail may lack luster, it is still shown to be an effective marketing tool even more so than Internet marketing. According to a recent DMA study, direct mail
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Help Your Employees Get Healthy, While Reducing Costs and Increasing Profits
Employee Health Strategies That Impact Your Bottom-Line
'There must be something I can do to address the rise in healthcare costs ' Like all business owners and leaders, you re searching for solutions to help rescue your company from the economic crunch. But you can only cut staff and spending so far. In the end, a healthier workforce will actually save money and deliver better results. To truly
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Using Sales Compensation Plans to Achieve Revenue Targets
One of the most critical decisions that a company makes is how to compensate its sales organization. Many plans don t align compensation reward with the desired sales activities, which leads to underperformance and frustration. When sales compensation plans are aligned with the goals of the company, the sales team has clear focus, motivation, and direction and the company gets the results it
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Help Your Employees Get Healthy, While Reducing Costs and Increasing Profits
Employee Health Strategies That Impact Your Bottom-Line
'There must be something I can do to address the rise in healthcare costs ' Like all business owners and leaders, you re searching for solutions to help rescue your company from the economic crunch. But you can only cut staff and spending so far. In the end, a healthier workforce will actually save money and deliver better results. To truly
more...
