From Web-based Seminars

Health Information Technology Introduction ...r health information technology systems will also benefit from our sessions to obtain basic knowledge to move forward in their project. Although there are no educational requirements for taking our workshops or courses, it is recommended that individuals either have healthcare experience and participate in electronic health record (EHR), and/ or health information technology (HIT)  more...

Health Information Technology Systems ...r health information technology systems will also benefit from our sessions to obtain basic knowledge to move forward in their project. Although there are no educational requirements for taking our workshops or courses, it is recommended that individuals either have healthcare experience and participate in electronic health record (EHR), and/ or health information technology (HIT)  more...

Inspired Goals Webinar YOU WILL LEARN: a The top three reasons why people dona ™t set goals a How to start fresh and complete past goals a The process of focus and attention a Goal setting tips a The language of goal setting a Strategy for what will likely stop you from achieving your goals a How to set goals that inspire and motivate a How to embrace failure and  more...

Project management Training Programs ... PMP ® Preparation Training (35 contact hrs) Commence from 21st April, '2012 7 Live Online Lectures on Saturdays and Sundays (Timings - 7. 30 PM to 10. 30 PM Indian Standard Time OR 2. 00 PM to 5. 00 PM GMT) Web based education program on a Agile Project Managementa (21 PDUa ™s) March 31st, April 1st, 7th & 8th '2012 (2 consecutive weekends) 4 Live Online Lectures on Saturdays and  more...

Live Online PMP Preparation Training from PMSoft Live Online PMP Preparation Training from PMSoft scheduled on 17th Sept. 2011  more...

Data Integration for Data Mining with Talend Open Studio OS ...rations included in the course are: Extraction of data from multiple input sources (tables, Excel, or delimited text files) Mapping several instances of records with the same information from fields of different names in different files to the same name in a common output file Transformation of fields to common formats, scales, and data types Output of a common data stream to a  more...

Oracle Developer Track 11g This course is for people either new to Oracle database or are trying to learn the new Oracle 11g database version. This instructor led course will take you from Basics to Advanced level of training. At the end you get experience certificate from us.  more...

Learn Web Design with UCSD Extension Digital Arts Center ...from a static to dynamic website using jQuery, JavaScript, MooTools, Flash banners and galleries, and CSS3. This is the second course in our Web Design Skill Series. Through the series, students will learn to hand-code their own websites. The first course in the series explains the hand-coding process, the second takes students from static to dynamic sites, and the third completes the process  more...

Learn the Essentials of Digital Design at UCSD Extension - Online Course A continuation of Digital Design Essentials A. Students will explore advanced applications of typography and color to improve upon and achieve effective visual communication. In addition, students will evaluate the properties of paper and its effect on the outcome of printed publications from an aesthetic and technical standpoint. Design projects will be developed working with real-time clients  more...

The Interactive Agency Emerging Media and Design - Online Course ... Raisch, this course is intended for creative individuals from digital arts, gaming, and immersive media who want to learn about emerging media from a digital perspective. First hand knowledge of the latest campaign strategies will be provided. Students will learn about digital campaigns, the latest advances in cross-device marketing, and what is happening in the marketing departments and ad  more...

Struggling to break into Clinical Research Informative webinar about the clinial research professions and the ways to break into the clinical research field. The webinar describes the pharmaceutical industry now and the future of the industry, the CRA job, skills and personality and how to break in the clinical research field. The session is live, so you can ask questions and get answers from the presenter, an experienced clinical  more...

Green Business Planning - Online Workshops ... Business Plan (An Online Workshop) Join Vic Desotelle from DiscoveryFuel. com for an online business planning series. http://discoveryfuel. com/ green-business-planning-workshops These workshops are for small business entrepreneurs who have dreamed of owning a sustainable business. Learn how to make a viable business plan that moves your green idea from conception to successful  more...

MS Project 2007 and 2010 Training in Kolkata Features of the MS Project Training by Simplilearn: a Two days Comprehensive class room training by Eminent trainer a Microsoft developed Audio-video course content and offline reference material a Access to e-learning content for 1 year a Help always just a click away! a Proven study methodology a More than 6000 PMP aspirants from across 108 countries have undergone a  more...

Navigating the Alphabet Soup of Employment Law - What Every Manager Needs to Know ... Law seminar will review the life cycle of Employment Law from hiring to firing and review the impact that each of the employment discrimination laws has on each phase of employment. Learn what you can legally say in your job postings, during interviews and in your employment application. Understand how to avoid discrimination in the workplace and how to prevent Employment Law liability for  more...

MANAGING LEAVE OF ABSENCE PART I - FMLA FMLA is one of the most complicated and legalistic laws out there. It is also one of the most important laws that you need to know about when managing an employee's leave of absence issues. Make sure that your managers and HR Managers understand how to ensure legal compliance with the FMLA. This webinar will provide our top tips for avoiding the FMLA mistakes that can cause legal liablity and  more...

GINA AND GENETIC INFORMATION AS A NEW PROTECTED CLASS - WHAT YOU NEED TO KNOW ABOUT THIS AND OTHER NEW PROTECTED CLASSES ... be prepared for the upcoming litigation that will result from the passage of the Genetic Information Nondiscrimination Act (GINA) that prohibits discrimination based on a new protected class a genetic informationa . This webinar will provide best practices to avoid violation of this new federal law as well as tips on methods to ensure compliance. In addition, this webinar will also cover the  more...

TOP 10 TIPS FOR CREATING A BLOGGING AND SOCIAL MEDIA POLICY ... The difference between an employer that is protected from the risks caused by social media and one that is not can be as simple as having a well-drafted social media policy. Learn the top 10 tips for creating a social media policy including the following: a Tips for Developing a Blogging and Social Media Policy a Doa ™s and Dona ™ts For What Should Be Included in the Policy  more...

From Hiring To Firing What Every Manager Needs to Know ...ment law seminar will review the life cycle of employment from hiring to firing and review the impact that each of the employment discrimination laws has on each phase of employment. This employment law Webinar is a must for small employers! A one hour and 15 minute on-line Webinar with ample time for questions and answers. Date: September 28, 2012 Time: 12: 00-2: 00 EST Cost: $199 per  more...

Employee Handbooks Dos and Donts ...mportant tool that an employer can have to protect itself from future liability. However, there are important mistakes that employers can make that reek havoc for employers. Learn what policies must be in your employee handbook as well as phrases and terms that you should never use in such a handbook. This informative seminar will outline for you the dos and dona ™ts of drafting an  more...

Top Tips For Managers to Prevent Harassment in your Workplace ...ironment sexual harassment. The webinar provides examples from actual court cases. It focuses on an employer's obligations when there has been an incident of sexual harassment as well as strategies on how best to prevent sexual harassment from occurring in the workplace. In addition, this webcast provides an in-depth discussion on other types of unlawful harassment under both federal and state  more...

Call Center Social Media Certification - Live Online - May 9-11 2012 Social media represents one of the most significant changes in consumer media behavior in history, resulting in fundamental shifts in the way companies communicate and interact with consumers. This course provides the practical knowledge and insights required to establish objectives and strategies and to properly select the social media platforms to engage consumers, while monitoring and measuring  more...

Call Center Workforce Management Certification - Live Online - August 1-3 2012 ...e managers covers the entire workforce management process from the gathering of data to the production of forecasts, schedules, and budgets. We include lessons that benefit attendees from any sized organization, large and small, with real-world examples of solutions that work in practice - not just theory. When this learning is expanded to workforce management, the focus extends to forecasts,  more...

Call Center Workforce Management Certification - Live Online - April 4-6 2012 ...e managers covers the entire workforce management process from the gathering of data to the production of forecasts, schedules, and budgets. We include lessons that benefit attendees from any sized organization, large and small, with real-world examples of solutions that work in practice - not just theory. When this learning is expanded to workforce management, the focus extends to forecasts,  more...

Listening for Tech Entrepreneurs Tech Entrepreneurs can be so steeped in their product that they don't pay attention to what is happening around them, then they wonder why they're not getting funding, a market, or customers. A major factor in this challenge is the lack of well developed listening skills. Many tech entrepreneurs have no idea how they listen, let alone if their listening habits are appropriate for the situation  more...

Documentum E20-120 Training This training includes: Documentum Fundamentals Documentum Development Documentum Administration. Documentum Foundations Classes, Documentum Foundation Services, Process Builder, Forms Builder. We also give training on Documentum 6. 5 with all new and advanced topics being covered. This is done both in physical and online mode. Trainer are all EMC certified professionals and working in  more...

Documentum 65 Training This training includes: Documentum Fundamentals Documentum Development Documentum Administration. Documentum Foundations Classes, Documentum Foundation Services, Process Builder, Forms Builder. We also give training on Documentum 6. 5 with all new and advanced topics being covered. This is done both in physical and online mode. Trainer are all EMC certified professionals and working in  more...

SOA BPEL Online Training ...y is the fact that it can help bind applications easily - from SAP to Oracle Apps to Siebel to PeopleSoft to Legacy Systems to .Net systems - now you can develop applications that span all the above and more. That too, using industry standard protocols like WSDL, HTTP etc. The idea is that each of the applications expose themselves as services that can talk the same language. And then we  more...

Word Processing for Law Professionals Webinar - featuring Microsoft Word 2007 The Principles of Legal Word Processing The Fundamentals of Microsoft Word The Perils of Direct Formatting From WordPerfect to Microsoft Word Styles: The Backbone of Document Formatting  more...

Introduction to Visual Basic 2008 Training ...udio profiles, XML comments, IntelliSense, and debugging. From there, you will learn all the Visual Basic 2008 language features that you must internalize in order to create full-featured Web or Windows applications that make best use of the .NET 3.5 platform.You will learn about data types, variables, and operators, along with all the important flow control structures. You ' ll work through  more...

Comprehensive Silverlight 2.0 Training In this Silverlight training course students will build an application through a series of hands-on labs. The first 3 days of the course focus on the basics of Silverlight and supporting technologies. The final 2 days focus on more advanced Silverlight-specific topics.While this course targets Silverlight developers, designers looking to utilize Silverlight and Microsoft  more...

Java Persistence with Spring ...upports a wide range of persitence technology: everything from raw JDBC to sophisticated object/relational mapping tools such as Hibernate and TopLink, and also the new Java standard for those tools, the Java Persistence API. We work at either end of this spectrum, with exercises on improving JDBC code with Spring templates and transaction management, and also how to integrate JPA entities and  more...

Object-Oriented Analysis and Design (OOAD) Training with UML ...se 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 suite for your organization. An emphasis is placed on Use Cases to  more...

Oracle Database 10g: Administration Level I In this database administration course students gain the skills necessary for basic day-to-day administration of an Oracle10g database. This Oracle training class is the starting points for Oracle database administrators and also sets the foundation for advanced administrator training and certification. The class target audience is Oracle database administrators.  more...

Oracle Database 10g: Administration Level II ...to Oracle database administrators is that of recovery from failure, especially if the recovery must not result in a loss of any data. This Oracle trainig class presents all the standard failure scenarios and the best recovery strategies for each. Strategies for on-line backups, complete and incomplete recovery, media recovery vs. flashback database recovery and many other  more...

MOC 8824 - Sales Order Processing in Microsoft Dynamics GP 10.0 ...o easily manage the life-cycle of your customer ' s order from the initial quote to the shipment documentation and final invoicing. You learn how to perform additional functions setting up process holds for quality assurance and linking order documents to purchase orders.A thorough understanding of these topics allows you to boost sales order processing productivity and help improve customer  more...

MOC 8400 - FRx 6.7 Report Design Essentials II ...ement reports. You learn how to use links to extract data from a variety of sources including non-financial metrics maintained outside the general ledger. This course also teaches you how to move into cutting edge technology, using OLAP and XRBL output options. These skills enable you to take control of the financial reporting process, allowing you to be more productive and efficient in the way  more...

MOC 6419 - Configuring, Managing and Maintaining Windows Server 2008 Servers ...mbines five days worth of instructor-led training content from the Network Infrastructure Technology Specialist, Active Directory Technology Specialist, and IT Professional Server Administrator courses of Windows Server 2008 to provide students with the knowledge and skills that are required to manage accounts and resources, maintain server resources, monitor server performance, and safeguard  more...

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  more...

MOC 4995 - Programming with the Microsoft .NET Framework using Microsoft Visual Studio 2005 ... .NET training class enables developers who are migrating from a different development language, an earlier version of Visual Basic .NET or Visual C#, or who have completed entry-level training and experience using Microsoft Visual Studio 2005, to gain in-depth guidance on programming the Microsoft .NET Framework versions 2.0 and 3.0 with Visual Studio 2005.This training class targets  more...

MOC 5051 - Monitoring and Troubleshooting Microsoft Exchange Server 2007 This Exchange Server 2007 training class teaches messaging specialists to monitor and troubleshoot an Exchange Server 2007 messaging system. Students will learn how to correlate client and server issues and resolve those issues. They will also learn how to monitor systems and create reports from the monitoring data.  more...

MOC 2261 - Supporting Users Running the Microsoft Windows XP Operating System This Windows XP training class provides students with the knowledge and skills to troubleshoot and escalate or repair problems with Windows desktop operating systems by reacting to incident requests from end users. This class will provide the basic knowledge of system architecture and security needed to provide the students with the requisite skills required to support end users and adhere to  more...

MOC 2262 - Supporting Users Running Applications on a Microsoft Windows XP Operating System This Windows XP training class teaches students how to troubleshoot and repair problems with Windows XP by reacting to incident requests from end users. The class will help the student prepare for Exam 70-272: Supporting Users and Troubleshooting Desktop Applications on a Microsoft Windows XP Operating System.  more...

Comprehensive JSP Training ...applications, and then covers JSP 2.0 features in detail, from scripting elements to use of dedicated JavaBeans to JSP expressions, and quick introductions of JSTL and custom tag development. By the end of the module students will be able to create their own JSP applications, including interactive applications using HTML forms and pages that perform fairly complex processing using scripts  more...

Java Swing Training ...ed, both handling AWT-style events, such as action events from button clicks, and handling events fired by the model that lies under a particular control. In the second module, more sophisticated and powerful controls are studied: the tree and table controls. Each is presented in a separate chapter, allowing students to dig into the underlying architecture and to develop a firm grasp of the  more...

Introduction to JavaServer Pages ...applications, and then covers JSP 2.0 features in detail, from scripting elements to use of dedicated JavaBeans to JSP expressions, and quick introductions of JSTL and custom tag development. By the end of the module students will be able to create their own JSP applications, including interactive applications using HTML forms and pages that perform fairly complex processing using scripts and  more...

Ajax Training ...er with JavaScript and to manipulate XML content returned from the server. Ajax opens the door to creating sophisticated web-based applications with much more of the logic (and therefore code) is handled on the client. While Ajax allows for more dynamic and responsive applications, it changes the traditional role of JavaScript dramatically and forces developers to rethink how they write and  more...

E-mail Etiquette Training ...mail accessories and passwords, and prevent your password from being stolen. Course activities also cover using the subject line, considering your recipient, managing e-mail volume, following netiquette guidelines, attaching files, preparing for recipient reactions, and using emoticons effectively. Students also learn about the differences between writing online and traditional paper-based  more...

Introduction to C# 2008 Training ...udio profiles, XML comments, IntelliSense, and debugging. From there, you will learn all the language features that you must internalize in order to create full-featured Web or Windows applications that make best use of the .NET platform.You will learn about data types, variables, and operators, along with all the important flow control structures. You will work through several examples  more...

Microsoft Business Intelligence from SQL 2008 through SharePoint and Office 2007 This Business Intelligence (BI) training class provides students with the knowledge and skills to develop Microsoft End-to-End business solutions using SQL Server 2008 in an integrated environment with SharePoint and Office 2007. The BI class introduces students to Microsoft Unified Data Model, SQL Server 2008 Analysis Services, Integration Services, Reporting Services, Report Builder 2.0,  more...

Windows Applications with Visual Basic 2008 Training ...set of new functionality for the Visual Studio developer. From new language features, including LINQ (Language Integrated Query), to new client-side data support, Visual Studio 2008 and the .NET Framework 3.5 make it easier than ever to create robust, enterprise-level applications. This Visual Basic 2008 Windows Applications training course begins with the basics. Students will become familiar  more...

Windows Applications with C# 2008 Training ...set of new functionality for the Visual Studio developer. From new language features, including LINQ (Language Integrated Query), to new client-side data support, Visual Studio 2008 and the .NET Framework 3.5 make it easier than ever to create robust, enterprise-level applications. This C# 2008 Windows Applications training course begins with the basics. Students will become familiar with  more...

Budgeting Training: Budgeting Basics ... budgets. Virtually every aspect of budgeting is covered, from preparing income statements and company expense reports, to developing your own personal plan. Students learn about different types of budgets and the elements of a successful budget. Students also learn how to create a budget, analyze and compare budgets, and create operating and manufacturing budgets. Course activities also cover  more...

Business Problem Solving and Strategic Decision Making This Business Problem Solving training course teaches students the fundamentals of solving business problems. This course introduces students to the need for problem solving, ineffective responses to problems, the elements of an effective solution, and the skills needed for effective problem solving. Students will also learn how to avoid inappropriate responses to problems, identify types of  more...

Strategic Decision Making Training This Strategic Decision Making training course teaches students how to plan, frame, and research decisions. Students learn how to define decisions, apply appropriate decisions frames, avoid overconfidence, deal with uncertainty, generate options and select the best one, develop numerous high-quality options, evaluate the options and make a final choice, review and learn from experience, identify  more...

Groovy Training for Java Developers This Groovy training course teaches experienced Java developers how to write programs in Groovy that simplify, enhance, and expand their existing systems. The course will be taught by Ken Kousen. Dr. Kousen is an instructor, consultant, and developer specializing in all areas of Java, XML, and, more recently, Groovy and Grails. Over the past decade, he has taught courses and made  more...

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  more...

Web Development using Grails This Groovy on Grails training course teaches experienced web developers how to use the Grails framework to rapidly create sophisticated web applications. The course will be taught by Ken Kousen. Dr. Kousen is an instructor, consultant, and developer specializing in all areas of Java, XML, and, more recently, Groovy and Grails. Over the past decade, he has taught courses and made  more...

Advanced Oracle SQL Training on Oracle 11g/10g The primary objective of this Oracle training class is to consider advanced subjects and techniques pertaining to the SQL database language. Even professionals experienced in other implementations of the industry-standard SQL language will benefit from the advanced and Oracle-specific features of SQL discussed in this course.  more...

MOC 6420 - Fundamentals of Windows Server 2008 Network and Applications Infrastructure This Windows Server 2008 training class introduces students to network and applications infrastructure concepts and configurations provided by Window Server 2008. Students will be able to acquire a fundamental understanding in order to pursue advanced topics available for certification in the network and applications infrastructure areas.This training class is intended for new IT employees or  more...

MOC 6421 - Configuring and Troubleshooting a Windows Server 2008 Network Infrastructure This Windows Server training class provides students with the knowledge and skills to configure and troubleshoot a Windows Server 2008 network infrastructure. Students will learn to implement and configure secure network access and implement fault tolerant storage technologies. Students will gain an understanding of the network technologies most commonly used with Windows Server 2008 and  more...

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  more...

MOC 5060 - Implementing Windows SharePoint Services 3.0 This SharePoint Services class provides students with the knowledge and skills to successfully implement Microsoft Windows SharePoint Services (WSS) version 3.0 in their organizations.The class emphasizes that students should think about the architecture of their entire environment, including business and application needs, during the planning and deployment phases. The course covers how to  more...

Visual Studio 2008 Training: New Features for Visual Basic Developers ... set of new functionality for the Visual Basic developer. From new language features, including LINQ (Language Integrated Query) to new client-side data support, Visual Studio 2008 and the .NET Framework 3.5 make it easier than ever to create robust, enterprise-level applications. This Visual Studio 2008 course, including full written courseware, demonstrations, and lab exercises, introduces  more...

Introduction to Microsoft Silverlight In this Silverlight training course students will build an application through a series of hands-on labs. The course focuses on the basics of Silverlight and supporting technologies.While this course targets Silverlight developers, designers looking to utilize Silverlight and Microsoft Expression Suite will also benefit from the knowledge gained.  more...

Advanced Microsoft Silverlight Training This advanced Silverlight training course focuses on more advanced Silverlight-specific topics. While this course targets Silverlight developers, designers looking to utilize Silverlight and Microsoft Expression Suite will also benefit from the knowledge gained.  more...

Visual Studio 2008 Training: New Features for C# Developers ...ds a large set of new functionality for the C# developer. From new language features, including LINQ (Language Integrated Query) to new client-side data support, Visual Studio 2008 and the .NET Framework 3.5 make it easier than ever to create robust, enterprise-level applications. This Visual Studio 2008 course, including full written courseware, demonstrations, and lab exercises, introduces  more...

Six Strategies to Grow Aggressively in the Federal Market webinar on June 14th 2012 ...or example, number two on the list, Octo Consulting Group from Vienna, Virginia, boasts an annual growth rate of 228%, growing in five years from $187 thousand to $22 million. Other companies on the list show meteoric growth, ranging from 60 to 326%. You yourself probably know some teammates that may have not made the list, but have done spectacularly well for themselves. However, your company  more...

Implementing Statistical process Control SPC for Short Run Production You are invited to attend the Manufacturing Executive Institutea ™s August 16th 2012 3rd Thursday - a Operations Improvement Seriesa FREE webinar, a Implementing Statistical Process Control for Short-Run Production.a SPC has helped many manufacturing companies achieve world class quality in production operations. Application of SPC techniques have become commonplace and a normally  more...

A Case for Routine Use of Statistical Process Control SPC in Manufacturing You are invited to attend the Manufacturing Executive Institutea ™s FREE June 2012 3rd Thursday - a Operations Improvement webinar, A Case for Routine Use of Statistical Process Control (SPC) in Manufacturing. Statistical Process Control is a term that describes a process for predicting failures and methodically determining the underlying cause(s) before the predicted failures can  more...

A Better Method for Cross Training Production Personnel ...ing a successful program with little or no involvement from HR. a How to identify the Job Masters and then get them to share their experiences and skills with others. a How to get employees to certify the skills of other employees. a Building an internal value system around breadth of individual capabilities equal to the one that is built around depth of capabilities. a  more...

Power of Persuasive Proposals Every proposal is first and foremost a sales document aimed to persuade the evaluators to award the contract to you. a Sellinga in proposals is often misunderstood, however, because it happens to be a dirty word for many technical, engineering, scientific, and government personnel. It is unfortunate because true selling in proposals doesna ™t look anything like whata ™s associated  more...

JIRA Fundamentals Training Course ...ectively. The material covers all features of the product from an end-user's perspective, and provides a solid foundation for users with all levels of experience, since it explains the most effective ways to use JIRA and some handy tips for getting the most value out of the software. Attendees from this session will become proficient with creating issues, using the workflow, assigning issues to  more...

Measuring Performance of Your Global Procurement Organization How to Shape Behaviours in Global Purchasing You are invited to attend the Manufacturing Executive Institutea ™s November 8th, 2011 a Global Manufacturing Enterprise Seriesa FREE webinar, a Measuring Performance of Your Global Procurement Organizationa How to Shape Behaviors in Global Purchasing.a This montha ™s powerful 1-hour webinar has 2 important objectives: 1. Define the best alternatives for structuring a  more...

Better Methods To Control Tools Fixtures in Production Manufacturing ANYTHING requires tools, fixtures and supplies; in addition to people, machines, materials and methods. And while most improvement initiatives focus on production methods and material availability, it is often the tools and fixtures that cause manufacturing disruptions, sometimes leading to shipping delays and customer dissatisfaction. How many times have you been ready to produce,  more...

Understanding Improving Yields Scrap Rework Scrap and yield are different measurements that tell us different things about our production processes. Measuring and monitoring them precisely (and individually) is an important component of any process improvement initiative. If these values get comingled in the measurement procedures, underlying root cause analysis is certain to result. This FREE 1-hour webinar presents the CORRECT  more...

How to Factually Evaluate Critical Supplier Performance and Risks ...to source significant amounts of materials and components from global suppliers and are creating substantial risks within their supply chains. Companies are discovering that sourced-material disruptions can and often do, result in dramatic and unfavorable impacts to material delivery reliability, total material cost and received material quality. GDI's Comprehensive Supplier Performance &  more...

How to Conduct an Effective Monthly Variance Review Meeting ...their direct reports to explain all significant variances from plan. These variances are usually, though not always, stated in terms of dollars. Specific variance that great plant managers have a tendency to routinely review, include: + Closed Order Variances + Purchase Price Variances (PPV) + Burden Absorption Variances + Labor Absorption Variances + On-Time Completion Variances +  more...

Confluence Fundamentals webinar ...course is a comprehensive view of the Confluence features from an end-user's perspective. The material provides a solid foundation for users with all levels of experience, and explains how to become a more active contributor in your enterprise wiki. Attendees from this session will become proficient with editing pages in wiki markup and rich text, embedding images, using macros, labels,  more...

JIRA Workflow Administration Webinar The JIRA Workflow Administration training course covers all administrative features of JIRA related to customisation of the workflow and data capture. Attendees from this session will become proficient with creation of custom fields, new issue types, workflow statuses, transitions, post functions, field configurations, mandatory fields, hidden fields, workflow schemes and applying a JIRA workflow  more...

Better Methods for Maintaining Accurate Operation Standards ...0: 00 AM PDT. Participate in this virtual training event from the comfort of your office or home computer. Learn from an expert instructor AND your industry peers! Manufacturing professionals ALWAYS worry that production operation standards are inaccurate. This is appropriate because operation standards are the cornerstone of successful capacity planning, work order control, process flow  more...

Constructing a Component Criticality Matrix A Better Way to Identify Important Components ...ble for managing thousands of parts that can be purchased from hundreds of Suppliers. The large number of parts and Suppliers makes it nearly impossible to manage each individual part as much as one wants to. This is why Procurement organizations rely upon stratification methods and other sorting methodologies to provide insights into GROUPS of parts. This way, the Purchasing professionals  more...

How to Achieve Maintain ERP Systems Master File Data Integrity You are invited to attend the Manufacturing Executive Institutea ™s May 19th 2011 3rd Thursday - a Operations Improvement Series FREE webinar, How to Achieve & Maintain ERP Systems Master File Data Integrity. Contrary to the popular belief that modern, fully-integrated information systems provide executives with the tools to make more effective and efficient decisions, there is increasing  more...

Preserving Precious Capital Attacking the SEVEN Most Significant Capital Wasters in Your Company Times are tough and capital preservation is at the top of every executivea ™s priority list. But specific techniques necessary to rapidly eliminate waste and reduce operating costs can be difficult to define and even more difficult to implement. If you manage ANY type of an organization, you have waste which steals precious capital from your enterprise. Now, more than ever, it is important  more...

A Better Method for Rationalizing Capital investmentsTools for Calculating REAL Investment Value It is an interesting observation that manufacturers continue to struggle with the best way to rationalize new investments in capital equipment. Interestingly enough, this struggle is often the result of failed cost accounting systems and methods. It is these systems that fail to provide accurate information that ultimately allow an investment to be appropriately modeled within the context of the  more...

Group Approaches with Trauma Survivors Explores clinical models of interventions for trauma survivor groups, including approaches with recovery and personal awareness components. Various types of program promotions and intake/ admission procedures will be addressed. OBJECTIVES: Group Work with Trauma Survivors explores clinical models of group intervention with trauma survivors. Therapeutic group approaches with recovery and  more...

Early Intervention Field Trauma Training ... mental health and health care professionals will benefit from Field Trauma training. This is an entry-level program and no pre-requisites are required to receive the Field Trauma designation other than successful course completion. Participants will learn about on-site responding and learn how to respond to a critical event and aid those requiring psychological first aid. Field Traumatology  more...

Demystifying the Calculations of Efficiency Utilization and Productivity ...ation of the formulas, we will explain how values derived from the formulas can be altered and how companies can benefit from the CORRECT understand of these terms. We will clearly show participants HOW to calculate these values and WHEN to use the results of the measurements. Though this webinar presents a seemingly simple topic, the correct understanding and use of efficiency, utilization  more...

Better Methods for Calculating Safety Stock Service Levels This FREE 1-hour webinar addresses some techniques for reducing safety stock and still meeting target customer service levels. Specifically, this program will present some new ideas in safety stock and service level management by utilizing a unique modeling instrument that simulates safety stock, service levels, stock-outs and inventory investment from a random stream of demand over multiple  more...

How to Calculate the Impact on Total Factory Costs from a One Percent Change in Planned Load ...binar, How to Calculate the Impact on Total Factory Costs From a 1% Change in Planned Load. The largest cost driver in most manufacturing companies, outside of the cost of direct material, is underutilization of semi-fixed and fixed costs. These costs are the aggregated expenditures on plant, property, people and equipment (PPP&E). For manufacturing companies to grow and sustain success,  more...

Manufacturing Opportunities in Costa RicaGateway to Enhanced Productivity and Lower Manufacturing Costs For North American companies looking for solid manufacturing capabilities at a low cost; or looking for a high productivity manufacturing location, Costa Rica offers some outstanding benefits. The Central America country of Costa Rica is more than a beautiful landscape in the middle of Latin America. It is also a country that boasts one of the most attractive industrial climates anywhere in  more...

Dental - Medical Cross Coding - Webinar By MentorHealth Medical Coding in dental practices is gradually becoming a necessity. Many dental practices have long been sheltered from having to explain to dental carriers why they performed the patients' procedures. They have simply submitted codes for the procedures that were performed. Wednesday, October 12, 2011 10: 00 AM PDT | 01: 00 PM EDT  more...

Statistical Procedures Needed for Compliance with the Guidance on Process Validation - Webinar By GlobalCompliancePanel Overview: This guidance document contains several statements that make it clear that statistical procedures will be expected. Recently, FDA issued new draft guidance on process validation. When finalized, it will supersede the previously issued guidance documents on process validation. It is expected that the final guidance will not be much different from the draft. Thursday, September 6, 2012  more...

GMP for Phase 1 Products - Webinar By GlobalCompliancePanel Overview: This presentation will cover the contents of the guidance that was given. FDA has issued as rule that relieves Phase 1 products from complying with the GMP given in 21 CFR 211. At the same time, they ruled that the products must continue to comply with the GMP as given in the Food, Drug, and Cosmetic Act. Guidance was then given to describe these GMP. Tuesday, August 7, 2012 10: 00  more...

The FDA Inspection Process From SOP to 483 - Webinar GlobalCompliancePanel Overview: Does the FDA call in advance or just show up at my door? Where do I let the inspector go? Do I give them a tour? What should I let them see? Who should I let them talk to? Are they ever going to leave? The FDA inspection is the most nerve-wracking event in the life of a regulatory professional - you're in charge of compliance, usually in the background, and NOW you're in the spotlight,  more...

Recalls Removals and Market Corrections in Compliance with FDA and ISO Requirements - GlobalCompliancePanel Overview: To satisfy QSR and ISO 13485 requirements, medical device companies must respond to field reports swiftly and compliantly. There are certain circumstances in which a report from the field requires the device manufacturer to take steps regarding product in the field. Wednesday, June 27, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

First in Class First in Man Compounds Targeting Tumor Bioenergetics from Lab Bench to Clinical Trials Working with the FDA to me Overview: Many anticancer drugs are not tumor selective. For chemotherapy the lack of drug and disease specificity and need for higher dosing leads to adverse and serious adverse events that may be dose limiting. Preventing a therapeutic level to be achieved in a patient. Thursday, June 28, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

Excel Spreadsheet Validation for FDA 21 CFR Part 11 - GlobalCompliancePanel Overview: 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.  more...

How to submit a 510k and get it cleared from FDA - Webinar By GlobalCompliancePanel Overview: This webinar is intended to demonstrate how submit a 510(k) and get it successfully cleared from the FDA. Thursday, June 28, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

RAPS Approved Seminar on Risk Management in Pharmaceutical Industry at Mumbai Overview: This training course has been designed to address the processes, methods, and tools associated with Quality Risk Management. It highlights the disciplined environment that is necessary for proactive decision making to continuously assess what risks a organization is exposed to, which risks are important to deal with and how the implementation of strategies can mitigate risks.  more...

Scale-Up Cycle Transfer and Maximum Throughput Capability for Lyophilized Products - Webinar By GlobalCompliancePanel Lyophilization cycle scale-up and cycle transfer between dryers has traditionally been one of the most challenging issues in manufacturing. Cycles that have been designed on development-scale equipment, and are producing acceptable product, can suddenly start suffering from both physical and chemical instability when scaled-up to a larger freeze-dryer, or transferred between production  more...

Residual Moisture Testing of Lyophilized Products - Webinar By GlobalCompliancePanel This webinar will cover the various methods used to determine residual moisture in products ranging from bulk powders, to sterile freeze-died products in vials, to foods. Understanding the different techniques, their limitations, and proper execution will result in more accurate and precise moisture results, which translates into better quality products with longer shelf lives. Tuesday, June  more...

Medical Device Supplier Quality Agreements - Webinar By GlobalCompliancePanel Overview: The FDAa ™s Quality System Regulation (QSR) explains how a device manufacturer must manage suppliers. This ranges from supplier evaluation and selection to control methods. One common approach uses a supplier quality agreement. This webinar explains the elements of a supplier quality agreement and its implementation. Wednesday, June 20, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

Learning from Recent FDA Warning Letters Related to Computer Validation and Part 11 - Webinar By GlobalCompliancePanel In July 2010, the FDA announced to conduct a series of inspections related to 21 CFR Part 11. In meantime the program is still on-going. FDA made it very clear that Part 11 is in effect and will be enforced according to original Part 11 and the guidance from 2003. Thursday, April 26, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

Pharmaceutical Water System Use Monitoring Avoiding Problems by Doing It Right The Practicality of Real-Time Release - Webinar ...from a pharmaceutical or other high purity water system, for use in manufacturing, cleaning or for sampling, is likely responsible for as much as 90% of all water system deviations. Done properly, it can lead to greatly reduced product or process contamination, improved water system control and avoidance of time-consuming and frustratingly inconclusive problem investigations. Tuesday, April  more...

Understanding Analytical Test Results Comparing Two Sets of Data - Webinar GlobalCompliancePanel Overview: The class will cover the understanding the properties of single test results and how they may be compared. There are many problems that arise from a misunderstanding of the properties of single data sets and the problems are compounded when data sets are compared. The discussion will cover the misconceptions and present methods to allow proper comparisons, while considering the risks  more...

Validation and 21 CFR Part 11 Compliance of Computer Systems - US Seminar 2012 at San Francisco Overview: In December 2010 the FDA changed the way it does audits to include 21 CFR 11 add-on inspections. Very little is known about this, yet the FDA has already issued citations on the subject. This Webinar will present the latest on FDA thinking (with slides directly from the FDA's Office of Compliance), discuss how these inspections will impact both your company an the industry, and provide  more...

Business Process Optimization in Pharmacovigilance - Webinar By GlobalCompliancePanel Overview: This webinar will describe how to assess and optimize Pharmacovigilance operations from cost effective, compliance, and safety perspectives. A structured methodology for assessing drug safety operations will be presented. This will include recognizing the need to conduct process analysis, developing and prioritizing project portfolio, performing the analysis, and finally implementing the  more...

Drug Development Process - From Discovery to Marketing - Webinar By GlobalCompliancePanel This webinar will provide a clinical and regulatory perspectives on requirements to take a new drug from research to market. Wednesday, February 15, 2012 10: 00 AM PST | 01: 00 PM EST  more...

Residual Moisture Testing - Proven Techniques - Webinar By GlobalCompliancePanel This webinar will cover the various methods used to determine residual moisture in products ranging from bulk powders, to sterile freeze-died products in vials, to foods. Wednesday, February 1, 2012 10: 00 AM PST | 01: 00 PM EST  more...

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,  more...

FDAs Revised Draft Guidance on Medical Device Changes and the 510k - Webinar By GlobalCompliancePanel This webinar will discuss the new draft guidance document from the FDA: "510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device", dated July 27, 2011. Wednesday, January 25, 2012 10: 00 AM PST | 01: 00 PM EST  more...

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  more...

Dietary Supplement Regulatory Compliance in the United States Labeling Product Claims Updates from the FDA - Webinar By GlobalC This 90 minute live, interactive webinar will review the dietary supplement regulations and discuss how to verify that your products are compliant, while citing differences with food and drug regulations. We will also cover what qualifies a material as a dietary ingredient, considerations for manufacturers and distributors, requirements for compliant labeling and acceptable marketing claims. An  more...

Dental Digital Radiography - Better for the Patient and the Practice - Webinar By mentorhealth This webinar is for those wondering what digital radiography is, how it differs from film, how it works, and how it impacts the dental office. And for those unsure which system to purchase and how to incorporate it into Their practice? It is also for those who are using it and learn how to use it more effectively. Tuesday, December 20, 2011 10: 00 AM PST | 01: 00 PM EST  more...

What is New in Ultrasonics Exploring Piezoelectric Technology - Webinar By mentorhealth ...what "the Piezo" is all about? What makes it so different from "the Cavitron"? This course is designed to examine the unique capabilities of piezoelectric ultrasonics and the role micro-ultrasonics play in contemporary periodontal therapeutics. Discussion of hand scaling versus power scaling will be explored, as well as an overview of the various piezoelectric ultrasonic devices that are on  more...

Hazard Analysis A practical guide - Webinar GlobalCompliancePanel Hazard analysis meetings, you have probably spent hours discussing whether a scenario is a hazard, or the cause of a hazard, or debating whether the probability of an unmitigated hazard is high or low, or went off on a tangent evaluating very unlikely hazard scenarios, or wrestled with group members who consider hazard analysis meetings a waste of time. Tuesday, December 6, 2011 10: 00 AM  more...

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.  more...

Calculating Overtime Correctly - Webinar By TrainHR ... well as its importance in avoidance of suffering damages from civil law suits. Why you should attend: Calculating overtime is simple, right? Ita ™s just time and a half! What is so tough about that? Not so fast. Overtime is based on the regular rate of pay, and calculating the regular rate of pay is more complex than it appears. Whata ™s included in the calculation? The  more...

Disaster Preparedness - How to be prepared for the unexpected - Webinar By mentorhealth Are you prepared enough to survive, let along successfully recover from a disaster? The physical devastating possibilities that can happen to your practice include fire, flood, earthquake, hurricane, tornado, tsunami, or worse. Wednesday, October 5, 2011 10: 00 AM PDT | 01: 00 PM EDT  more...

ITIL v3 Service Operation Virtual Instructor Led ...xploration of the new and updated topics in ITIL ® v3 from the point of view of the owner of a process or set of activities. The course is intended for those who work within a Service Operation (SO) environment and require a deeper understanding of the underlying concepts, processes/ functions and activities involved and management responsibilities and how they may be used to enhance  more...

Effective Internal Auditing-Making Quality Systems More Efficient for the Medical Products Industry - Webinar By GlobalComplianc The different types of internal audits and how they are approached will be discussed. The Internal Audit Lifecycle will be followed from beginning to end. It will be shown that. Internal audits are not simple exercises to determine compliance to some regulatory standards. Instead, the focus must be on auditing the company's quality system to determine if they are meeting their objectives and are  more...

The FDA Inspection Process From SOP to 483 - Webinar By GlobalCompliancePanel This webinar will provide valuable assistance to all companies that market in the U. S., since they are by definition subject to FDA regulation, in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields.  more...

How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant - Webinar By GlobalCompliancePan This Webinar deals with what happens, and under what circumstances, when the protocol is not followed (PNF) and why this is of particular significance. Covered, will be how a protocol deviation with the least significant effect where there is no substantive effect on the risks to research participants, no substantial effect of the value or integrity of the data, and did not result from willful  more...

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  more...

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.  more...

SAP FICO Online Competency Development Training program .../ Reconciliation account/ sales inv posting 20. Payments from Customers/ Open item management/ Discount allowed/ Dunning 21. Special G/ L transactions/ Define Dunning Procedure/ Assign Dunning Procedure 22. Asset Accounting- Sub Ledger 23. Chart of Depreciation/ Depreciation Area/ Assign COD to Company Code 24. Assign Input tax indicators/ Account Determination/ Asset Class/ Number range  more...

JAVA J2EE JEE Professional Role Based Training from Zaran Tech TRAINING DETAILS: Course Duration: 80 hours Training + Actual project Case Studies + Assignments 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  more...

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:  more...

Business Analyst Competency Development Program ...iness Analyst Training uses best practices and guidelines from International Institute of Business Analysis (IIBA ®) in their Business Analysis Body of Knowledge ® (BABOK ® v2. 0). The training content is customized to meet the practical needs of a Business Analyst professional. In this training, attendees learn: 1. Introduction to Business Analysis 2. Understanding and  more...

How to Survive a DEA Inspection Series Only Manufacturers and Distributors - Webinar By GlobalCompliancePanel This training will cover DEA record-keeping and security requirements that a registrant must comply with when handling controlled substances and regulated chemicals. It covers elements of what occurs during unannounced DEA Diversion inspection and the auditing of all controlled substances and regulated chemicals. As a firm handling those products, you will get a better understanding of what is  more...

A Simpler Approach to Implementing or Validating CGMPs to 21 CFR 11 Electronic Records Signatures - Webinar By GlobalComplianceP ...ing software vendor claims to separate compliant software from "vaporware". A manufacturer is responsible to identify these requirements and implement them into an effective 21 CFR Part 11 CGMP software V&V process. Why you should attend: Software has become pervasive in medical product manufacturing documentation and cGMP compliance actions, and in the controlling, running and monitoring  more...

Requirements of validation and control of EO Sterilization - Webinar by global compliance panel Sterilization validation is a topic that results in many audit observations from the FDA and international regulatory bodies.  more...

Practical Laboratory Statistics ...asic spreadsheet functions to compare data sets generated from many different kinds of test equipment. Why Should You Attend: Most people hate statistics, because they don't understand statistics. If you either generate or review laboratory data, you will want to attend this seminar. We will discuss the basics in a way that doesn't involve lots of jargon and complicated equations. We use  more...

FDA Inspections - Dos Donts - webinars by gcp The purpose of the FDA inspection is a verification activity that should demonstrate to the regulatory agency and provide assurance that products consistently meet quality expectations and that your company is operating in a consistent and compliant state of control.  more...

HIPAA Accounting of Disclosures Expanded scope in proposed rule means new obligations The session will walk the listener down the path from the current HIPAA Accounting of Disclosures rule, through the HITECH Act's required changes, and the into the proposed rule to implement HITECH which goes beyond what was required in the law and establishes a new right to an Access Report of all electronic PHI.  more...

HIPAA Accounting of Disclosures Expanded scope in proposed rule means new obligations by gcp The session will walk the listener down the path from the current HIPAA Accounting of Disclosures rule, through the HITECH Act's required changes, and the into the proposed rule to implement HITECH which goes beyond what was required in the law and establishes a new right to an Access Report of all electronic PHI.  more...

Validating Radiation Sterilization for Medical Device Industries by gcp ...dation is a topic that results in many audit observations from the FDA and international regulatory bodies. Proper understanding of the principles and requirements of the related standards is crucial to proper compliance. In addition, understanding the requirements and integrating them early in the product design can lead to quicker time to market. This seminar will help RA/ QA staff understand  more...

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...

W-2s 1099s Independent Contractors Protect Yourself with Proper Classification by TrainHR Understanding proper classification requirements and helping to guide your company through this sensitive and important decision can be one of the most valuable and beneficial services that payroll departments can provide to the organization. Can you be relied upon to make those determinations correctly?  more...

Breakthrough Performance Management that is Practical Effective and User-Friendly ...are fully capable of producing good outcomes, but benefit from leadership and support that helps them take action in the best possible manner. The employee and manager form a performance partnership and jointly agree on the performance targets and the actions necessary to achieve them. Using a simple but effective protocol and checkpoints along the way, the manager is assured that the employee  more...

The Law and Psychology of Mental Health Issues at Work Substance Abuse Depression and the Bermuda Triangle of the ADA the FMLA a This workshop helps HR professionals understand how to navigate the difficult and often murky challenge of dealing with "invisible disabilities." To make matters more confusion, the recent amendments to the A. D. A. have a significant impact on the rights of mentally employees as well as the responsibilities of employers. This practical workshop address both the legal and psychological issues  more...

Preventing Harassment in the Workplace by TrainHR ...e workplace. It will review the laws protecting employees from harassment and the recourses employees have. It will define who is covered and describe the two main kinds of sexual harassment in the workplace. It will cover what should be in an effective Harassment policy, how it should be communicated, and who is held responsible for assuring compliance. Also included is handling complaints,  more...

Effective Employee Performance Documentation Elements and Techniques by TrainHR ...municate better, improve performance, and defend yourself from legal challenges by producing more effective performance documentation. Employees are more productive when they know what is expected of them. Employee discipline is easier when documents are in order, and high standards are met when directions are clear. Learn simple, stress-free methods for collecting the right information,  more...

Dress Code Nightmares How to Deal with them and How to Prevent them by TrainHR This practical webinar teaches HR professionals and small business owners how to avoid harassment or discrimination claims that can arise from poorly handled - or inconsistently enforced - dress code issues. It provides specific guidance on how to talk about some of the most difficult topics there are - body odor, inappropriate dress, an unkempt appearance, etc.  more...

Emotional Intelligence What it is and Why it Should Matter to You by TrainHR The most important "e-term" you may learn in 2011 is emotional intelligence. Experts say it can make or break careers and elevate executive leadership to higher levels of success, so what are the best moves and worst emotional pitfalls you can make? Learn from executive coach and nationally acclaimed author Arnold Sanow what it is and why it matters to the success of executives and the companies  more...

Failure Mode Effects Analysis FMEA - The Tool of Choice to Improve Product and Process Reliability and Efficiency While Reducin ...sfaction, by proactively addressing failures that keep us from meeting critical customer requirements in processes or products. It reduces product development costs operational risk. Join Dr. Anthony Tarantino, a Six Sigma Master Black Belt for an interactive session to learn how and when to deploy FMEA in your organization. He will also present an innovative means to combine FMEA with a new  more...

Information Security Risk Analysis Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePane ...d in the preamble to the HIPAA Security Rule and guidance from the US Department of Health and Human Services. Areas of high risk, as identified by respected industry organizations, will be identified to ensure that the most significant risks are discovered and adequately prioritized. The risk analysis process will be applied to a simplified example in order to relate the process to a real  more...

Pharmaceutical and Medical Device Validation Guidances - Similarities and Differences - Webinar By GlobalCompliancePanel ... validation is and how you would explain it to an "alien" from another industry? Now, this is not to mean that other industries do not practice process validation because they do. It is that in the manufacture of medical products, so much is at stake for the professional and their patient. It is imperative that medical products must perform consistently so that patients can be treated in a  more...

Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel ...hasis is placed on ethical, moral, and legal expectations from the FDA. Why Should You Attend: The webinar is designed for mid-level Quality Engineers and Quality Engineers who design and manage the Quality system. What you will learn: * The CAPA definition * the CAPA LIFE cycle * Tools for each CAPA cycle * CAPA requirements * Tools for Preventive Action  more...

Developing the Master VV Plan to Meet US FDA ISO 13485 and 14971 Requirements - Webinar By GlobalCompliancePanel ... / structure * Product Validation a how it differs from process / equipment V&V * Process / Equipment / Facility Validation - FDA's new guidance * When and How to use DQ, IQ, OQ, PQ, or their equivalents * How to use Product Risk Management Tools (per ISO 14971 and ICH Q9) * The 11 key documents for software validation * Incorporating 21 CFR Part 11 requirements  more...

Recalls Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel ...: 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 website  more...

FMEA and Risk Management for Medical Devices - Webinar By GlobalCompliancePanel ...Devices, all facets of risk management must be considered from cradle to grave. The term "Risk Analysis" is no longer appropriate for medical device manufacturers and has been replaced by "Risk Management". Areas Covered in the Session: * Failure Mode Analysis Terms * Risk Management and FDA * Risk Management in Design Control * Risk Management & ISO 14971 * Risk  more...

21 CFR Part 11 How to Successfully Prepare for and Host an FDA Inspection - Webinar By GlobalCompliancePanel ... time is of essence, having an ability to access records from any location around the world is more critical then ever, and for the same reason, electronic records will be more needed and desired in each organization. In addition, approval of documents and records in a timely fashion is absolutely needed at all times, and being able to do just that via an electronic media is understood. For  more...

Internal 21CFR Part 11 Compliance Auditing of Computer Systems - Webinar By GlobalCompliancePanel ...er systems in compliance with 21CFR Part 11." These words from an FDA or state regulatory inspector can send shivers down your spine. Are you ready for an internal QA or FDA inspection at your site? Areas Covered in the Session: * 21CFR Part 11 Compliance * Review of the regulations * Regulatory requirements * Site Inventory * Compliance Assessment * Risk  more...

Key Factors to Write an Effective Standard Operating Procedure SOP and Work Instructions WIs - Webinar By GlobalCompliancePanel ... is also designed to help differentiate Work Instructions from Standard operating procedures. Attendees will learn the steps used to write effective work instructions and Standard operating procedures. Why Should You Attend: The current shift in FDA thinking is that manufactures do not give their employees enough direction to perform their jobs. This thinking is reflected in many warning  more...

The Most Common Problems in FDA Software Validation Verification- Webinar By GlobalCompliancePanel ...ing to audit an internal IT system, anticipating an audit from a customer, preparing for the inevitable FDA inspection, or a vendor wishing to clearly demonstrate a software product is Part 11 compliant, this teleconference will give both old hands and new staff the practical information needed to understand the applicable regulations and solid methods to document compliance. * FDA  more...

How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel ...ectives: * Learn what FDA expects and will request from you during your DHR review. * How QSIT inspections related to record keeping is performed by FDA. * How Change can affect DHRs. * Learn what constitutes a good DHR procedure. * Learn how risk management fits into DHR compliance. * Learn how to better audit quality record systems. Areas Covered in the  more...

Understanding Attribute Acceptance Sampling including Z14 and c0 Plans -- Webinar By GlobalCompliancePanel ...ides a complete description of Z1. 4, showing the process from receiving the lot to selecting the sample size to making the accept/ reject decision. We will discuss the following issues: * How to use the sampling tables to determine the sampling plan * Ways to avoid common errors and misunderstandings with the sampling tables * The difference between single, double, and  more...

Requirements of the Master Production Record - Webinar By GlobalCompliancePanel ...e area of production records. With the information gained from this presentation, your company's policy or standard for MPR's will comply with the regulations and you can be assured that you will be working within the intent of and meeting these regulatory requirements. Most importantly, by complying with these regulations, you are ultimately helping to provide a better product for your  more...

The Pharmaceutical Quality System - Webinar By GlobalCompliancePanel ...many other concepts. Individuals in pharmaceutical firms, from the highest executive to the middle manager are wondering how these will fit into their organization and its Quality system, and how they will impact them, personally. This webinar will help the participants understand what a Pharmaceutical Quality System is and how to transition from the compliance systems of today to the  more...

A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - W ...eds. 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 the compliance based Pharmaceutical GMPs with the Medical Device Quality System Regulation. ICH-Q7A will be included because it is a cross between the quality and compliance approach. This webinar  more...

Navigating the Regulatory Environment for the Implementation of Alternative Microbiology Technologies - Webinar By GCPanel ...ocusing on RMM implementation * Current perspectives from the U. S. Food and Drug Administration (FDA), European Medicines Agency (EMA), Australian Therapeutic Gods Administration (TGA) and the Japanese Pharmaceutical and Medical Devices Agency (PMDA) * Use of comparability protocols * Submission strategies * Concept of research exemptions Who Will Benefit: *  more...

Controlled Substances and the Hospital Pharmacy - Webinar By GlobalCompliancePanel ...overs the storage and dispensing of controlled substances from the pharmacy to the many sections within the hospital including patient wards, emergency rooms and surgical areas. * DEA Recordkeeping Requirements: This section covers the required records to be maintained in order to comply with DEA regulations. Records include receiving/ shipping order forms and invoices, inventories, drug  more...

Validation of ExistingLegacy Computer Systems for FDAEU Compliance - Webinar By GlobalCompliancePanel ...A warning letters * Industry recommendations, e. g., from the GAMP * Assessment activities, e. g., gap analysis and risk assessment * Reviewing and updating the validation master plan for existing systems * Going through the validation lifecycles from planning to ongoing tests in routine use * Documenting validation results for FDA/ EU compliance * Dealing with  more...

HIPAA Business Associates How the regulations have changed and what you need to do for compliance now - Webinar By GCPanel ...the law and the proposed regulations and what has changed from the old rules. * The suggested and required content for a compliant business associate agreement will be presented. * Issues of how to assign liability and costs in the event of a breach will be discussed. * Current BAs will learn what they have to do to get their contractors established as their business associates.  more...

HIPAA Breach Notification What to do to prevent breaches and what to do when they happen to you - Webinar By GCPanel ...t and how entities are doing it. We'll cover the guidance from the US Department of Health and Human Services that shows how to encrypt so as to prevent the need for notification in the event of lost data. * We'll discuss how to create the right breach notification policy for your organization and how to follow through when an incident occurs. In addition, a policy framework to help  more...

Off-Label Promotion of Medical Devices Maximizing Your Performance Claims within FDAs Framework of Acceptable Practices - Webina ...hasis is placed on ethical, moral, and legal expectations from the FDA. You will improve your understanding of regulatory expectations for your products and improve promotional compliance for released products. The webinar is designed to help attendees understand the "off-label statute" and its legal implications. It is is also designed to help attendees operate within off-label promotional  more...

FDAs New Process Validation Guidance - Webinar By GlobalCompliancePanel ...l device division. The new requirements expand validation from a one-time activity into a full lifecycle philosophy, encompassing statistics, risk management, project management, and new technologies. No one involved in process development and validation in the drug, API, or biologics industries (or their vendors!) can afford to miss this presentation; while validation personnel in the medical  more...

Validating Rapid Microbiological Methods - Webinar By GlobalCompliancePanel ...(IQ, oq and PQ) * Pharmacopoeia testing requirements from the United States and European Pharmacopeias (USP and Ph. Eur.) * Acceptance criteria Who Will Benefit: Senior management and laboratory personnel responsible for the conduct of microbiological testing and microbial control strategies in manufacturing and product/ process development: * Microbiology * Quality  more...

The Investigation System Discovery Planning Root Cause Analysis CAPA - Webinar By GlobalCompliancePanel ...opics will examine each step of the investigation process from failure identification and notification through documentation. Participants will review root cause analysis techniques and observe how to identify corrective and/ or preventive actions towards successful remediation and closeout. This high-level overview will provide clarification on the steps of an effective investigation, what  more...

Understanding the Calibration Curve - Webinar By GlobalCompliancePanel ... these concepts by examining several real-world data sets from a variety of different analytical instruments. Why should you attend: Everyone who works with analytical data is working with a calibrated measurement system. However, few people really understand the principles and assumptions behind the calibration methods used for their instruments. As a result, we often make mistakes,  more...

Process Validation for Medical Devices - Webinar By GlobalCompliancePanel ...h a high degree of confidence that all manufactured units from successive lots will be acceptable. Successfully validating a process reduces the dependence upon in-process and finished device testing. Routine finished device testing is often insufficient to assure product quality. In some cases, destructive testing is required to show that the manufacturing process is adequate. End-product  more...

How to use QSIT to Your Advantage - Webinar By GlobalCompliancePanel ...eminar: * History of FDA inspection methodologies, from haphazard to QSIT. * Anticipate and prepare for FDA inspection. * Identify what inspectors look for during a QSIT inspection. * In depth analysis of the 4 major subsystems. * Review of remaining subsystems. * Knowing how to utilize the QSIT approach in internal auditing. Who will benefit: During FDA  more...

FDAs Proposed Rule Regarding Device Establishment Registration and Listing and How to Register and List - Webinar By GlobalCompl ...ions to facilitate FDAa ™s collection of information from foreign establishments regarding their devices that are imported into the U. S. as required by the 2002 Bioterrorism Act and other proposed changes to be addressed. The Proposed Rule, if finalized, would require establishments to provide additional or different information than specified in the current regulations, but which FDA now  more...

Medical Device Recalls How to Manage Them and Recent Trends - Webinar By GlobalCompliancePanel Overview: Medical devices are classified into three classes, Class I, II, and III, based on the level of control necessary to assure the safety and effectiveness of the device. Recalls of Class II devices represent 61% of all device recalls over a review period, followed by Class III devices at 28%. This Webinar will provide a recent update on the latest trends and causes for device recalls and  more...

Off-Label Promotion of Drugs - Regulatory Documents Explained - Webinar By GlobalCompliancePanel ...aintiffs' verdicts in products liability cases that arise from the off-label uses of their products. The pharmaceutical industry has been distributing reprints of scientific and journal articles on off-label uses of drugs for many years now, but the regulations and rules in recent years were burdensome, and the Department of Health and Human Services Office of the Inspector General (OIG) has  more...

XML Training ...L Advantage of XML Where is XML used? Show the Demo from Google/ Amazon Webservices 3. USING XML IN APPLICATIONS Separates Data Simplifies Data Sharing Simplifies Data Transport Simplifies Platform Changes Makes Your Data More Available Used to Create New Internet Languages 4. VIEW AND EDIT XML FILES Sample XML file Viewing XML files List of Browsers Editing  more...

Project Management for Clinical Trials - Webinar By GlobalCompliancePanel ...which will include the following: * Obtain a brief from the Project Sponsor which defines the clinical trial objectives, rationale, outline timeframe, and estimated budget available * Review literature and other available information * Discuss the therapeutic areas with experts in the company and externally such as key opinion leaders, patient groups may also be of help *  more...

Tougher US FDA cGMP Compliance Audits - When Youre Not Ready - Webinar by GlobalCompliancePanel ...ession: * Key cGMP issues * Avoid complacency from past "good" FDA/ ISO audits * The desired response * How to respond now -- where to shift focus first * Where to direct scarce resources; A risk-based phased approach * How to address known problem areas during an Audit * Prove 'in control' * Maintain 'the edge' Who Will Benefit: * Senior  more...

Networking Basics Overview to computer networking Network Fundamentals Basic Troubleshooting Skills  more...

Redhat Linux Redhat Linux Administration Introduction to Unix Introduction to Redhat Linux Manage File Systems RPM Administration ( Package ) System Boot and Shutdown User and Security Administration Managing and Monitoring System Processes with CLI Tools and /proc System backups and Restores Network Administration  more...

Information Security - Overview ...ns protecting information and information systems/ assets from unauthorized access, use, disclosure, disruption, modification or destruction. Every individual who deals with information should have a better understanding on how to safeguard his/ her personal or company's data. This session will assist partcipants to 1. Understand WHAT, HOW & WHY of information security. 2. Plan further  more...

WorkPlace Skills A set of skills that are essential to success in the work life. These are very basic and fundamental skills one should possess to be successful in job selection or to succeed in his/ her work atmosphere. 1. Email and Telephone etiquette 2. Using MS Excel 2007 / 2010 3. Using MS Word 2007 / 2010 4. Using MS PowerPoint 2007 / 2010 5. Using emails - Webmails, Outlook etc., 6.  more...

Computer Basics Computer Fundamentals 1. Overview to Computers. 2. Computer Architecture. 3. Hardware & Software. 4. Managing your computer hardware 5. Adding hardware  more...

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.  more...

Excel Spreadsheets and FDA Device Regulations - Webinar by GlobalCompliancePanel ... Validation tools and how to use them to prevent the user from entering incorrect data. We explain the use of Formula Auditing to help ensure the calculations are performed correctly. Lastly, we explain the use of Protection to prevent inadvertent and unauthorized changes. To satisfy the broadest interest, we use Excel 2003 to illustrate the tools. The seminar shifts to the regulations for  more...

Understanding the Technical Requirements of 21 CFR Part 11 - Webinar by GlobalCompliancePanel ...l requirements of Part 11, to ensure system are compliant from a Part 11 technical perspective and, when coupled with sufficient procedural controls, will result in an overall Part 11 compliant deployment. Why should you attend: With the announcement in 2010 of a new Part 11 Inspection initiative, life science organizations can expect to see a higher level of scrutiny of the compliance of  more...

Practical Laboratory Statistics - Webinar by GlobalCompliancePanel ...asic spreadsheet functions to compare data sets generated from many different kinds of test equipment. Why Should You Attend: Most people hate statistics, because they don't understand statistics. If you either generate or review laboratory data, you will want to attend this seminar. We will discuss the basics in a way that doesn't involve lots of jargon and complicated equations. We use  more...

Effective Corrective and Preventive Actions CAPA 10 Steps to Success - GlobalCompliancePanel Virtual Seminar - Webinar By Global Overview: This CAPA training program helps you to understand, in 10 easy steps, the entire CAPA process. It includes elements of Quality Tools, Team Effectiveness, Awards & Recognitions, and Verification & Validation of actions taken. Attend this webinar to grasp the A to Z of CAPA and learn how to implement & manage it for success. Why Should You Attend: We have found out, through auditing  more...

Utilizing Good Requirements as a Foundation for the Effective Validation of PDMA-related Computerized Systems - Webinar By Globa .... The result is a validation effort that can be optimized from both a cost and time perspective. This webinar will provide a methodology for developing quality requirements for PDMA systems and will examine the benefits of leveraging those requirements to plan and drive the validation effort. Why should you attend: With the FDA announcing that it will be performing Part 11 audit this year  more...

Medical Device Changes and The 510k - Webinar By GlobalCompliancePanel ...ughen" the 510(k) process. A review of recent information from the Agency, including last summer's Working Group findings on the 510(k), Vol. I, as well as other goals of the Agency that have already been translated into action in the past year will provide direction in areas of concern and what to expect in the future. This will be performed by a review of FDA-stated areas of required review  more...

Validating Excel and Word Applications Documents - Webinar By GlobalCompliancePanel ...483 and Warning Letters indicating, and what can we learn from these? * What benefits beside regulatory compliance can be achieved for a company? Areas Covered in the Session: * Tougher FDA and EU MDD Software V&V Expectations * Key COTS Software Apps V&V Requirements * Problem Areas * Product, Equipment/ Process, QMS and Apps Software and Part 11 Requirements  more...

Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel ...ir notified bodies are no different. How can this be done from a project's inception? How can a Project Leader or Project Manager ensure critical elements are not omitted until late in the project when disaster looms? How to minimize scope creep? How to conclude a project "on time" and "within budget"? How to gain management support for the Milestones, Tasks, and Timelines? Use the Plan as a  more...

Effective Training Practices for FDA Compliance - Webinar By GlobalCompliancePanel ...ntation. By examining the GMP expectations on training from different regulatory bodies (from the regulations and citations), attendees will be able to envision what to include in a GMP training program. In addition, an overview of the training system, including types of training planning, will offer considerations to make GMP training more effective. Why you should attend: Regulatory  more...

Legal Risks in Social Media for Healthcare Providers - Webinar By GlobalCompliancePanel ...m. Areas Covered in the Session: * Legal issues from the public's perspective * Legal issues from the organization's perspective * HIPAA issues impacting social media marketing * "Spam" issues * Advertising rules * Content ownership and control * Potential SEC issues relative to social media marketing * Company-sponsored blogs versus outsider forums  more...

Preparing for GFSI and other Third Party Audits - Webinar By GlobalCompliancePanel ...cility's ability to achieve the maximum benefit and score from the audit. Why you should attend: More and more customers are requiring GFSI audits such as ISO 22000, BRC and SQF or accepting them in lieu of their own audits. Without passing scores on these audits, companies are losing current accounts and are denied access to new accounts and business. Many organizations are new to the  more...

Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations - Webinar By GlobalCompliancePanel Overview: Recent Consent Decrees have included requirements that the firm develop and implement systems that result in timely and complete investigations of deviations and corrective and preventive actions that address the root cause of deviations. FDA 483 and Warning letter observations identify inadequate investigations and follow-up. This webinar addresses adequate investigation of  more...

Using Foreign Trial Data in Your NDA Approval Process - Webinar By GlobalCompliancePanel ... While the law allows 100 percent of pivotal data to come from foreign trials, there have been very few such submissions accepted by FDA - mainly in limited therapeutic areas. Given lower costs and shorter recruiting times, the use of foreign sites is appealing to all drug developers, especially generic and 505(b)(2). Due to shortcomings found during site inspections, lack of inspection  more...

Complying with HIPAA Security Rules Whats in the rules and how you can most easily prepare for compliance - Webinar By GlobalCom ...eglect penalties that begin at $10, 000 minimum and go up from there. You need to be sure that you have completed an information flow analysis and a risk analysis and put in place the proper protections to secure protected health information, and documented all your policies and procedures, as well as any actions taken pursuant to your policies and procedures. What's more, with the breach  more...

Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel ... * Water System Microbial Control Myths o WFI from RO o Turbulent Flow and Flow Rate o Dead Leg Rules o Smooth Surfaces o Periodic "Sanitization" of 80 C Systems o In-Line Sterilizing Filters o Ozone as an Added Substance * Microbial Enumeration Myths o Referee Methods o Thermophiles in Hot  more...

Electronic Raw Data in Regulated Environments - Definition Recording and Archiving - Webinar By GlobalCompliancePanel ...curity and availability of records during the entire life from generation to deletion. While the intent is the same for all regulations only FDA's 21 CFR Part 11 and the EU equivalent Annex 11 have well defined requirements but still leave a lot of room for interpretations. Reference material for easy implementation: * SOP: Recording of GLP and GMP Raw Data. * SOP: Retention and  more...

Operational Risk Management Ensuring Safety for Food Systems - Webinar By GlobalCompliancePanel ...implement and can be implemented as a result of attention from any level in the operation. Generally, personnel in any operation can be employed in the risk reduction planning and implementation efforts. The session will also provide information regarding how to reduce supplier risk levels. Why you should attend: Management from any food handling company interested in learning a basic  more...

Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Webinar By GlobalCompliancepanel ...audit by reviewing and analyzing recent GCP audit finding from Clinical Investigators (Sites), Sponsors, and Institutional Review Boards (IRBs). Why you should attend: Quality assurance is defined as a "systematic and independent examination of trial-related activities and documents" that allows an auditor to determine whether or not the clinical trial was conducted according to the  more...

Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel ...regulations. It should be remembered the regulations came from industry and furthermore, that the regulations are the minimum requirements. When the pharmaceutical GMP's were issued, it was frequently stated that the regulations would result in only a mediocre or average quality system. This is because more emphasis would be placed on meeting the demand of the regulation, than studying the  more...

Understanding and Preparing for FDAs New Part 11 Inspection Program - Webinar By GlobalCompliancePanel ...ections: Preparation, conducts, follow up * Learning from past Part 11 inspections * Scope of the new Part 11 program: time frame, expected outcome * Criteria for selection of target companies * What inspectors are looking for * How to prepare your company for the upcoming inspections * Learning from previous inspections with focus on Part 11 and computer  more...

Key Concepts in Successful Water System Sanitization - Webinar By GlobalCompliancePanel ...his understanding to solve microbial problems originating from poor sanitization practices * Debunk a few water system myths related to sanitization Who Will Benefit: This webinar will be valuable for all companies that operate WFI or Purified Water systems, particularly for those in FDA, EMA, and AAMI regulated industries, including Medical Devices, Diagnostics, Pharmaceuticals, and  more...