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From Predictive Analytics World
Predictive Analytics World CONFERENCE VIDEOS DC Sessions Now - Online On Demand
...eos of PAW Washington DC, October 2010, including over 30 sessions and keynotes that you may view at your convenience. Access this leading predictive analytics content online now:
View the PAW DC session videos online
Trial videos a view the following for no charge:
a Keynote from Andrew Pole of Target: "How Target Gets the Most out of Its Guest Data to Improve Marketing ROI"
a
more...
Predictive Analytics World CONFERENCE VIDEOS DC Sessions Now - Online On Demand
...eos of PAW Washington DC, October 2010, including over 30 sessions and keynotes that you may view at your convenience. Access this leading predictive analytics content online now:
View the PAW DC session videos online
Trial videos a view the following for no charge:
a Keynote from Andrew Pole of Target: "How Target Gets the Most out of Its Guest Data to Improve Marketing ROI"
a
more...
From QLogy Management Services Pvt. Ltd
ITIL V3 Foundation Training in INR 2000


QLogy Offers ITIL V3F eLearning with 100% Passing Warranty....Pay just INR 2000 + 10. 3% S. T...
If you are already ITIL V3 Foundation Certified go for ITIL Advance module.
We are the only Company in INDIA to provide all the ITIL INTERMEDIATE MODULES.
We provide TWENTY Sample papers, but you can pass by solving just SEVEN,
Quality of eLearning can be judged by listening to FREE sample
more...
ITIL V3 Foundation Training in INR 2000
From American Medical Institute
CPR First Aide Universal Precautions Combo Class
...dents must pass the online test and then attend a skill
session to perform and review skills.
To earn AED certification, students must
have current CPR certification, AED Essentials test and attend a
skill session to perform and review skills. CPR certification is valid for 1
year. Basic First Aid certification is valid for 3 years. Universal Precautions
certification is valid for 1
more...
From Bureau Veritas Training
FREE - FSSC 22000 Food Safety Training - Webinar



ISO 22000 is the Food Safety Management System Requirements and PAS 220 is the Requirements for Prerequisite Programs. Both standards combined, with 2 extra requirements, equal the FSSC 22000 standard.
This Webinar will start at 11: 00 AM (Central USA Standard Time) on Friday, October 28, 2011 and be presented by Patrick Bele, Bureau Veritas Food Safety Program Manager and Senior Lead Auditor.
more...
From Statistics & Analytics Consultants Group
Introduction to Surveys





...
Each day will consist of four approximately equal-length sessions; the first session of the day will commence at 9: 00 a. m. and the final session will end at approximately 5: 00 p. m. The sessions will mix lecture presentations with practical work using software; tutorial help will be liberally available. Practice data sets, instruction guides, and a full set of notes will be provided. A
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From Kogent
BOI300 - BusinessObjects Data Integrator XI 3x - Core Concepts - Virtual Session
...ssObjects Data Integrator XI 3x - Core Concepts - Virtual Session
BusinessObjects Data Integrator XI 3. 0 enables you to integrate disparate data sources to deliver more timely and accurate data that end users in an organization can trust. In this three-day course, you will learn about creating, executing, and troubleshooting batch jobs, using functions, scripts and transforms to change
more...
BOC310 - Crystal Reports - Report Design I - Fundamentals of Report Design - Virtual Session
...Report Design I - Fundamentals of Report Design - Virtual Session
Crystal Reports 2008 is a powerful, dynamic, actionable reporting solution that helps you design, explore, visualize, and deliver reports via the web or embedded in enterprise applications. This two-day instructor-led course is designed to give you comprehensive skills and in-depth knowledge to plan and create reports that
more...
From Data-Scribe (r)
CiviCRM Next Level Training

Once you've attended our Getting Started with CiviCRM introductory workshop, you might want more in depth training on specific areas of CiviCRM. Our additional training levels would be a great follow-up for you.
Training can be held privately for individuals or groups. You also can attend an upcoming public session, which is held in a Webinar format.
more...
From Global Innovative Campus
Fundamentals of Engineering FE Exam Preparation - Civil Engineering Discipline - Afternoon Session 32 PDHs
Course Code: FE002
Date: 09 Oct - 17 Oct 2010
Location: Edmonton, AB
Details: Global Innovative Campus
10810 119 ST NW
Edmonton, AB
T5H 3P2
-- Satur/ Sun
Oct 09 / 10
Oct 16 / 17
Schedule: 8 hours / day
8: 30am - 5: 00pm
more...
From Single Sourcing Solutions, Inc
Authoring with Arbortext Editor (Tutoring)





A customized version of the "Authoring with Arbortext Editor" course, this mentor-led, one-on-one, individual instruction is tailored to the needs of the student and focused on their individual, personal skill development.
This course emphasizes hands-on experience, interaction between student and mentor, in a tutoring-like environment. Although the course is compressed, you will learn the
more...
From Future Media Concepts
Editing with Avid Media Composer v35 - Online
This course provides students with exposure to the core skills, workflow, and concepts involved in nonlinear editing on an Avid system. Session time is divided between demonstration and hands-on practice, with ample time for experimentation with sample material.
more...
From Healthcare and Medical Information Solutions
Health Information Technology Systems


...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) acquisition, use,
more...
From PMSoft Consultancy Pvt. Ltd
PMP Guidance Session
Live online Guidance Session for PMP Aspirants, who are interested in appearing for PMP Examination. Those who have doubts in their mind about the examination, PMI membership, eligibility, cost, training period etc. can ask questions directly & get the answers immediately by attending the session.
This is a free session to educate the people about PMP (Project Management
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From Advanced Clinical Research Services Inc>
Struggling to break into Clinical Research


Free informative webinar about the CRA profession 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 research
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From HR Learning Center LLC
LABOR RELATIONS TRAINING
One of the most difficult things for managers to do is to manage effectively in a represented environment. This is all the more true when your managers, who were used to managing in a non-represented environment, all of a sudden have to deal with labor relations issues for the first time. We will assist your managers in dealing effectively with the labor relations process and will provide an
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From Webucator
MOC 8811 - Foundation I in Microsoft Dynamics GP 10.0
This Microsoft Dynamics GP Foundation training class explores the basic elements of Microsoft Dynamics GP. Topics covered during this session include: system and company setup procedures, how to use reports and inquiries, how to use SmartList to expand inquiry and analysis capabilities, business alerts, process server and tips for the user to personalize shortcuts and checklists to streamline
more...
Introduction to EJB 3.0
This course introduces the experienced Java developer to Enterprise JavaBeans -- the Java EE standard for scalable, secure, and transactional Java components. EJB 3.0 has reinvigorated this area of Java enterprise development, with dramatic improvements in ease of use and smooth integration with servlet-based or JSF web applications. This course treats the 3.0 specification, with a few notes on
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Presentations: Preparing, Developing, and Delivering
This training course introduces students to the fundamentals of creating a presentation. Students will discuss the components of a good speech or presentation, and then they will learn how to develop their own. As students work through the activities, they will write and deliver three short presentations in class. They will be introduced to a variety of delivery techniques that include building
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From Pix Software
JIRA Fundamentals Training Course
Course Summary
The JIRA Fundamentals training course provides the ideal jumpstart for your team to use JIRA more effectively. 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
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Confluence Fundamentals webinar
The Confluence Fundamentals training 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
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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
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From GlobalCompliancePanel
New Final HIPAA Amendments New final rules for HIPAA Expand the Scope and Increase Responsibilities
...y do business in their facilities.
Areas Covered In the Session:
The new regulations will be reviewed and their effects on usual practices will be discussed, as well as what policies need to be changed and how.
We will show what policies and evidence you need to produce if you are audited by the HHS Office of Civil Rights. Now that there is a legislative mandate to audit compliance, and a
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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...
Risk Management in IEC 60601-1 Third Edition - Webinar By GlobalCompliancePanel
...requirements of the new standard.
Areas Covered in the Session:
ISO 14971 compliance is a requirement of IEC 60601-1
The new standard uses risk management throughout
The new standard is less prescriptive in many areas
The new standard requires that all applicable collateral and particular standards must be used for compliance
Current activities leading to full implementation of the
more...
HIPAA Security Rule Compliance When Communicating with Patients Using Mobile Devices - Webinar By mentorhealth
The session will discuss the requirements, the risks, and the issues of the increasing use of mobile devices for patient communications and provide a road map for how to use them safely and effectively, to increase the quality of health care and patient satisfaction.
Tuesday, November 29, 2011
10: 00 AM PST | 01: 00 PM EST
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Telecommuting Effective Policies Practices and Program - Webinar By TrainHR
This session will also cover how employees might approach their management with a proposal to adopt either a full telecommuting plan or hybrid and how to measure and justify positive results. This webinar will contain an overview of how to develop a policy
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Calculating Overtime Correctly - Webinar By TrainHR
...in this information packed event!
Areas Covered in the Session:
How to calculate the regular rate of pay
The eight narrowly construed exceptions to inclusion of payments in the regular rate
When you must include a bonus in calculating your employeea s overtime pay
How to handle overtime calculations once you've determined that a bonus qualifies as includable wages
How to
more...
Introduction to Contamination Control Master Plans - By GlobalCompliancePanel
...c contaminants for your products.
Areas Covered in the Session:
What is a CCMP and how is it valuable to my company?
What topics are covered in the CCMP and to what extent?
How is the CCMP controlled and updated?
How is the CCMP implemented?
Who contributes to the CCMP?
Who Will Benefit:
QA personnel
Regulatory personnel
Operations managers
Microbiologists
R&D Scientists
more...
Intelligent Routing for Temperature Sensitive Goods - Webinar By GlobalCompliancePanel
The session will cover strategies to provide real-time cold chain temperature tracking and traceability.
more...
Excel Spreadsheet Validation to Eliminate 483 - Webinar By GlobalCompliancePanel
This interactive webinar provides explicit details and live demonstration followed by a collaborative workshop that explains how to configure and validate a GxP compliant spreadsheet application.
What makes this session unique is the combination of step-by-step instructions and the hands on workings of each participant. Bring your laptop and use Excel for yo
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From ZaranTech.com
JAVA J2EE JEE Professional Role Based Training from Zaran Tech
... 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: Weekdays and Weekends after work hours.
ABOUT THE TRAINER:
1. Worked in various domains like Insurance, Financial / Banking, Retail, Auto, Telecom
2. Extensive experience in IT and Non IT projects as Sr.
more...
SAP BOBJ with BW integration Online Competency Development Training program
... 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: Weekdays and Weekends after work hours.
ABOUT THE TRAINER:
a More than 12 years of Consulting & Teaching experience in different modules of SAP BW versions (2. 0B, 2. 1, 3. 0B, 3. 1C, 3. 5, BW 7. 0 NW 2004S), BPC,
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From GlobalCompliancePanel
A Simpler Approach to Implementing or Validating CGMPs to 21 CFR 11 Electronic Records Signatures - Webinar By GlobalComplianceP
...nstrained industrial environment.
Areas Covered in the Session:
Verification or Validation
Current Regulatory Expectations and Recent Audit "Hot Buttons"
The Part 11 Project Validation Plan
The Simplified Approach to 21 CFR Part 11 Compliance and Software V&V
When and How to Use DQ, IQ, OQ, PQ (or their equivalents)
Simplified Sample V&V Test Cases and their Development
The FDA's 11
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
...into the design inputs correctly.
Areas Covered in the Session:
Introduction
Terminology / Definitions
Radiation characterization / effectiveness
Process Equipment
Product and Material Issues
Process Definition
Validation IQ/ OQ/ PQ
Documentation, review and approval of validation
Routine Monitoring
Product Release
Maintenance of process effectiveness
Who Will Benefit:
RA
more...
Breakthrough Performance Management that is Practical Effective and User-Friendly
... with employees. Day-to-day supervision, ongoing feedback sessions, and periodic formal discussions are combined into an integrated management model that is simpler, more effective and less time consuming. The secret ingredient to successful performance management is employee involvement in defining, tracking, and measuring the success of the work involved. The performance conversations
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Document Retention and Destruction
...d for any audit of your records.
Areas Covered in the Session:
Where records should be kept
What belongs in a personnel file
Keeping and maintaining legal records
Payroll and taxes
Back- up systems
Critical incidents files
Documenting oral and electronic communications
Security of files
Archive methods and back-up systems
Who Will Benefit:
Chief Human Resource Officers
HR
more...
Winning Presentation Skills Put Power Punch and Pizzazz into Your Presentations by TrainHR
If you want to project poise and professionalism, captivate your listeners, persuade people to act on what you say and develop comfort and confidence this session is for you.
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Failure Mode Effects Analysis FMEA - The Tool of Choice to Improve Product and Process Reliability and Efficiency While Reducin
Failure Mode and Effects Analysis is a tried an proven technique to improve the quality, reliability and safety of products and processes in a proactive manner.
It has been used successfully for over 60 years in very type of industry and in all stages of product development, process improvement projects. It helps to increase customer satisfaction, by proactively addressing failures that keep us
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Master Production Record Requirements - Webinar By GlobalCompliancePanel
This program will address the 21CFR and Eudralex Volume 4 requirements and interpretation, as well as FDA Guidance regarding the creation, review and approval, and control of Master Production Records.
The material will enable attendees to establish a consistent approach to the design of MPR, including cover page content, instructions, processing requirements and limits, and signature
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HIPAA Enforcement and Compliance Audits What the auditors want and how to be ready before they call - Webinar By GlobalComplianc
...session we will discuss the HIPAA audit and enforcement processes and how they apply to covered entities and business associates.
We will explain the enforcement regulations and their recent changes that increase fines and create new penalty levels, including new penalties for willful neglect of compliance that begin at $10, 000. We will discuss what information and documentation needs to be
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Good Documentation Practices for Laboratory Operations - Webinar By GlobalCompliancePanel
... look for during a lab inspection
Areas Covered in the Session:
21CFR and Eudralex references to documentation
Correcting errors and omissions
Dates and formats
Meanings of initials and signatures
Use of "NA"
Comments and explanations
Handling raw data (charts, strips, printouts)
Blanks
Entering numerical data
OOS Documentation Expectations
more...
DHF DMR DHR Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel
...velopment and/ or updates to both
Areas Covered In the Session:
* The U. S. FDA's DHF
* The EU's MDD and the Technical File / Design Dossier
* Design Control vs. a Product 'Snapshot in Time'
* DHF "Typical" Contents
* TF / DD Expected Contents
* Parallel Approaches to Documentation -- Teams
* Future Directions
* FDA and NB Audit Focus
Who will
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HIPAA Security Policies and Procedures Making them useful and relevant as well as compliant - Webinar By GlobalCompliancePanel
...policy details that are required.
Areas Covered in the Session:
* Find out what are the requirements for policies and procedures and why they're a good thing.
* Learn how having good policies and procedures and good documentation can make compliance easier.
* Learn the set of policies that need to be included in four groups of policies: Information Security Management
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Information Security and Payment Card Rules Protecting Patient Payment Data and Complying with PCI - Webinar By GlobalCompliance
...session, attendees will learn what the PCI DSS requires for protection and how the PCI DSS relates to the HIPAA Security Rule - there are substantial similarities, and being prepared for one helps you prepare for the other, as well as for other requirements, such as breach notification. We will discuss how the regulations and standards work and their legal basis, as well as provide up-to-date
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Information Security Risk Analysis Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePane
...session will present the background of the regulations that call for information security risk analysis and show how it fits in to an overall information security management process. The risk analysis process will be presented within the context of the overall risk prioritization and risk mitigation process, using an example.
The Information Security Risk Analysis Process presented utilizes
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The GCPICH Obligations of Sponsors Monitors and Investigators - barriers and solution - Webinar By GlobalCompliancePanel
...#153;s Monitors are so important.
Areas Covered in the Session:
* The historical background of why the GCP standards were developed
* The concept of and the purpose of a GCPa
* The thirteen ICH Principles of a GCPa
* The ICH definition of a GCPa and how it is applied
* The Regulatory requirements to follow to be GCP compliant
* Who, in the clinical
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Pharmaceutical and Medical Device Validation Guidances - Similarities and Differences - Webinar By GlobalCompliancePanel
...reat, cure, and diagnose disease.
Areas Covered in the Session:
* Defining IQ/ OQ and validation and its role in maintaining product quality
* Roles and responsibilities in the validation process
* The process validation lifecycle from design to product discontinuation
* How about Process Analytical Technology (PAT)
* Similarities and Differences-Product and
more...
Auditing an Active Pharmaceutical Ingredient API Contract Manufacturing Organization CMO - Webinar By GlobalCompliancePanel
...is critical to your supply chain.
Areas Covered in the Session:
* Examine key elements of an API audit
* Audit preparation
* The audit itself
o Opening Session
o Audit itself
o What to look for?
o Discussion of findings
o Suggestions and experience
* Closing Meeting
* Who should participate in audit
* Who
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Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel
Overview: CAPA is the most audited Quality subsystem in any Quality system. Most of the warning letters written by the FDA in 2010 were CAPA relate. Avoiding FDA CAPA findings starts with the design of a robust CAPA SYSTEM.
The webinar covers "Off-label statute" and the FDA's nonbinding off-label guidance as relates to re-prints, performance claims, and Promotion. Emphasis is placed on ethical,
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Develop and Execute the Company Software VV Program - Webinar By GlobalCompliancePanel
...nstrained industrial environment.
Areas Covered In the Session:
* Verification or Validation
* Current Regulatory Expectations and Recent Audit "Hot Buttons"
* The Project Validation Plan
* Product and Process / / Facilities / Equipment Software V&V
* When and How to Use DQ, IQ, OQ, PQ (or their equivalents)
* GAMP / Other Considerations
* The FDA's 11
more...
Root Cause Analysis - The Heart of a Successful CAPA Program - Webinar By GlobalCompliancePanel
...ng, implementation and execution.
Areas Covered In the Session:
* Regulatory "Hot Buttons"
* The 4 Basic Steps to Problem Solving
* A Suggested Investigation Template
* ID / Document the Problem
* Investigation / Analysis Methodology - The 7 RCA "Tools"
* Find the Solution(s)
* Monitor for Effectiveness
* Lock In the Change - Close the Loop
*
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Developing the Master VV Plan to Meet US FDA ISO 13485 and 14971 Requirements - Webinar By GlobalCompliancePanel
...front V&V planning and execution.
Areas Covered In the Session:
* Verification or Validation - Recent regulatory expectations
* The Master Validation Plan / 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
*
more...
Recalls Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel
... available to firms' competitors.
Areas Covered in the Session:
* Complaint definitions - FDA, Canada & Europe
* FDA's complaint handling requirements
* Canada & European Union complaint handling
* FDA's voluntary & mandatory reporting
* 21CFR 803, 806 & 810 explained
* FDA regulatory actions against firms
* Adverse event reporting - Canada & Europe
more...
FMEA and Risk Management for Medical Devices - Webinar By GlobalCompliancePanel
...en 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 Management in Design Control
* Risk Management & ISO 14971
* Risk Management & Medical Device Directives
Who Will Benefit:
* Regulatory Professionals
more...
21 CFR Part 11 How to Successfully Prepare for and Host an FDA Inspection - Webinar By GlobalCompliancePanel
...mply with the Part 11 regulation.
Areas Covered in the Session:
* Short and quick overview of the Part 11 regulation
* Detailed description of HOW TO prepare for an FDA inspection
* When and Where Part 11 is in scope or the scope of the inspection;
* Detailed description of HOW TO handle the FDA inspection during the inspection itself;
* Some trends when it comes
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Internal 21CFR Part 11 Compliance Auditing of Computer Systems - Webinar By GlobalCompliancePanel
...A 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 Assessment
Who Will Benefit: The employees who will benefit include:
* End-users responsible for applications that need to be validated
* QA managers and
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Key Factors to Write an Effective Standard Operating Procedure SOP and Work Instructions WIs - Webinar By GlobalCompliancePanel
..., and what a Work Instruction is.
Areas Covered In the Session:
* How to write a work instruction
* How to write a standard operating procedure
* Properties of an effective work instruction
* Properties of an effective Standard operating procedure
* The differences between work instructions and Standard operating procedures.
Who will benefit:
* Quality
more...
Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine
... and maintaining them in the DHR?
Areas Covered in the Session:
* FDA Quality Systems Regulation Requirements/ Definitions
* MDD Requirements/ Definitions
* Design History File (DHF)
o Definition
o Typical contents
o DHF and outsourced design/ production
o DHF and OEM relationships
* Device Master Record (DMR)
o
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Conducting Successful Product Complaint Investigations - Webinar By GlobalCompliancePanel
...ely and effective investigations.
Areas Covered in the Session:
* Understand how and why CAPA is tied in to product complaint investigations
* Examples of tools currently being used to conduct investigations
* How far and in-depth do you go with your investigations
* What are current FDA "hot" buttons and trends
* Benchmarks and best practices for investigations
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How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel
...ter audit quality record systems.
Areas Covered in the Session:
* Introduction
* Guidance documents/ QS regulation
* Major FDA 483 points
* Trends in FDA warning letters
* Determining best practice for the DHR audit
* Be prepared by knowing how to conduct a MORE thorough record audit
* FDA 483 point issuance prevention
Who Will Benefit:
* Senior
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Data Security Analysis for Healthcare Providers - Webinar By GlobalCompliancePanel
...et HITECH and HIPAA requirements.
Areas Covered in the Session:
* "Meaningful Use" data security analysis requirements
* HIPAA risk analysis requirements
* Methods for building a customized analytical tool
* Questionnaires and forms
Who Will Benefit:
* Healthcare providers
* Healthcare privacy officers
* Healthcare security officers
* Hospital
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Webinar on Cloud Computing SaaS - Webinar By GlobalCompliancePanel
...fully controlled by the client, since the vendor is in possession of servers and software. Cloud computing is cheaper in the long run, but the quality of validation does not have to be affected by this price cut. Vendors can provide validated systems that can be configured by the client and the client can leverage the validation effort performed by the vendor, which will also provide a cost
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Understanding Attribute Acceptance Sampling including Z14 and c0 Plans -- Webinar By GlobalCompliancePanel
... * Can you improve the process?
Areas Covered in the Session:
* Sampling concepts
o With or without replacement
o Simple or stratified sampling
* The binomial distribution
o Possible outcomes and Bernoulli trials
o The binomial formula and what it means
o The cumulative binomial
* Sampling plans
o The AQL
more...
Requirements of the Master Production Record - Webinar By GlobalCompliancePanel
...on to learning what is meant by "list of components", the session will cover attachments and documentation expectations. Finally, the webinar will review the process and requirements for issuance and handling of Batch Production Records (BPR), and clearly describe the difference between the master and the batch production record.
Why should you attend: All the requirements for the master
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Best Practices for the Implementation and Use of Test Management Tools - Webinar By GlobalCompliancePanel
...Automated Testing considerations.
Areas Covered in the Session:
* System Based Test Tools vs. Paper Based Test Tools
* Paper Based Validation Practices vs. System Based Test Tools
* Test Management Tool Implementation Considerations
* Test Management Tool Usage Considerations
* Automated Testing Considerations
Who Will Benefit:
* IT Managers and System
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FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP
... CRO's Monitors are so important.
Areas Covered in the Session:
* What doe the FDA look at when Auditing/ Inspecting a study?
* The Sponsor's responsibility in monitoring study conduct
* Components of a sponsor monitoring system beyond SOPs
* The nature of adequate oversight of all staff and non-staff
* The importance of Protocol knowledge in preventing errors
more...
Gowning Systems Used in Cleanrooms Controlled Environments - Webinar By GlobalCompliancePanel
...istent manufacturing environment.
Areas Covered in the Session:
* Identify what garment systems are available.
* Identify and discuss good and bad cleanroom gowning.
* Identify gowning techniques and sequence.
* Discuss what role each garment part plays in contamination control and human safety.
* Explore expectations of cleanroom garment suppliers.
* Discuss
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Facilities Cleaning in Cleanrooms and Controlled Environments - Webinar By GlobalCompliancePanel
...tent, and frequencies.
It is a very practical training session intended to assist personnel involved in the design, cleaning, monitoring, and assessment of cleanroom cleaning procedures. The key benefits of this course are:
* In-dept understanding of cleanroom cleaning methods.
* Achieve satisfactory inspections more easily.
* Higher assurance of new medical product
more...
Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel
...al Instruments to USP Categories
Areas Covered in the Session:
* Operational lab equipment requirements for calibration and qualification
* Most common inspection problems
* USP Chapter : Analytical Instrument Qualification
* Development of an effective equipment qualification master plan
* Calibration/ qualification phases: design qualification, installation
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The Use and Mis-use of FMEA in Medical Device Risk Management - Webinar By GlobalCompliancePanel
...e real value of the FMEA process.
Areas Covered in the Session:
* What is an FMEA
o What are the components of an FMEA?
* How should I use FMEA in performing risk management?
* What are the problems with FMEA in risk management?
* How is an FMEA conducted
o What and who are needed
o Identifying significant risks
o Development
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Understanding ISO 13485 vs ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel
Overview: ISO 13485: 2003 is a quality management system standard specially written for the medical device industry and is on the U S Food & Drug Administration (FDA) list of recognized consensus standards.
Medical device firms certified to ISO 13485: 2003 will find themselves very closely compliant with FDA's Quality System Requirements under 21CFR 820. This presentation will help you to
more...
Good Documentation Practices for GMP Operations - Webinar By GlobalCompliancePanel
...d limit expression determinations
Areas Covered in the Session:
* 21CFR Part 211 and Eudralex references to documentation
* Correcting errors and omissions
* Dates and formats
* Meanings of initials and signatures
* Use of "NA"
* Comments and explanations
* Handling raw data (charts, strips, printouts)
* Blanks
* Entering numerical data
Who
more...
A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - W
...uestions are strongly encouraged.
Areas Covered in the Session:
* Module 1 - Introduction to Quality and Compliance Concepts
* Module 2 - Differences between Medical Devices and Pharmaceuticals
* Module 3 - Scope of the GMPs and the Quality Cycle
* Module 4 - Standards of Quality
* Module 5 - The Shifting Paradigm to Focus on Customer and User Satisfaction- The
more...
Navigating the Regulatory Environment for the Implementation of Alternative Microbiology Technologies - Webinar By GCPanel
...at your manufacturing facilities.
Areas Covered in the Session:
* Review current regulatory status of rapid method acceptance
* Regulatory publications and presentations focusing 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
more...
Elements of the Lot Disposition Process - Webinar By GlobalCompliancePanel
...sound quality management systems.
Areas Covered in the Session:
* Compilation of Completed Records
* Quality Technical Agreements
* QA review of production records
* Laboratory Testing Results
* Batch Production Record Review
* Critical Utilities and Environmental Monitoring Data
* Requirements for COA
* Communication
* Lot disposition
Who
more...
Validation of ExistingLegacy Computer Systems for FDAEU Compliance - Webinar By GlobalCompliancePanel
...ve Validation of Computer Systems
Areas Covered in the Session:
* Definition of legacy systems and retrospective validation
* FDA requirements and inspection practices
* Examples of FDA warning letters
* Industry recommendations, e. g., from the GAMP
* Assessment activities, e. g., gap analysis and risk assessment
* Reviewing and updating the validation master
more...
HIPAA Business Associates How the regulations have changed and what you need to do for compliance now - Webinar By GCPanel
...ew responsibilities and obligations for HIPAA BAs.
The session will provide attendees the following tools, benefits, and solutions:
* The audience will learn how business associates are now handled under 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.
more...
Regulatory Complaint Handling Vigilance Recalls - Webinar By GlobalCompliancePanel
Overview: Improper complaint handling can result is serious regulatory problems as well as hitting the bottom line. Recalls, FDA Warning letters & even seizures could result.
This presentation will review the regulatory requirements for complaint handling and adverse events reporting in the USA, EU & Canada. Suggestions for investigating and documenting complaints & pitfalls will be included.
more...
Overall Residual Risk Evaluation - Webinar By GlobalCompliancePanel
...Overall Residual Risk Evaluation.
Areas Covered in the Session:
* Choosing the Evaluation Team
* Determining the Evaluation Process
* What documents should be part of the review?
* Using the Risk Chart in the review
* How to compare to the Risk Acceptability Criteria
* Documenting the results of the Evaluation
Who will benefit:
* Risk Managers
*
more...
Documentation for IEC 60601-1 3rd Edition Compliance - Webinar By GlobalCompliancePanel
... as additional time requirements.
Areas Covered in the Session:
* Requirements of IEC 60601-1 Third Edition
* Required use of Collateral standards
* Required use of Particular standards
* Required use of ISO 14971 Risk Management
* Use of IECEE Test Report Forms
Who will benefit:
* Compliance Engineers
* Project Managers
* Quality Engineers
more...
Developing the Risk Management Plan - Webinar By GlobalCompliancePanel
... in compliance with the standard.
Areas Covered in the Session:
* ISO 14971 requirements for risk management planning
* Setting Risk Acceptability Criteria
* Planning for verification of risk control implementation and effectiveness
* Documenting responsibilities for risk activities
* Establishing risk review activities
* Example of a risk management plan
more...
FDAs New Process Validation Guidance - Webinar By GlobalCompliancePanel
...ith the release of this standard.
Areas Covered in the Session:
* Specific discussions include
* Background of the original guidance, its history, application, and items covered
* FDA regulatory authority
* Growth of competing standards and the competing expectations of the medical device industry
* The history and philosophy of the new guidance
* The three
more...
Validating Rapid Microbiological Methods - Webinar By GlobalCompliancePanel
...and the PDA Technical Report #33.
Areas Covered in the Session:
* Learn how to develop a validation strategy
* User requirements specifications (URS)
* Design Qualification (DQ)
* Supplier assessment/ audit
* Functional design Specifications (FDS)
* Requirements Traceability Matrix (RTM)
* Developing test plan, including installation, operational and
more...
Excel Spreadsheets Step-By-Step Instructions for Compliance - Webinar By GlobalCompliancePanel
...GxP compliant spreadsheet application.
What makes this session unique is the combination of step-by-step instructions and the hands on workings of each participant. Bring your laptop and use Excel for your own needs. This session will make you a better Excel user, saving you time and costs.
Areas Covered in the Session:
* Develop spreadsheet applications that are GxP compliant.
more...
Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel
... to perform a validation project.
Areas Covered in the Session:
* Learn which documents the FDA expects to audit.
* How to use the risk-based validation approach to lower costs.
* How to link requirements, specifications, risk management, and testing.
* Document a computer system validation project using easy to understand fill-in-the-blank templates.
* Based on:
more...
The Investigation System Discovery Planning Root Cause Analysis CAPA - Webinar By GlobalCompliancePanel
... analysis for corrective actions.
Areas Covered in the Session:
* Elements of a thorough investigation process (Discovery through Closeout)
* Identifying the Problem
* Introduction to Root Cause Analysis
* Define corrective action and preventive action
* Effective Documentation of the Investigation Process
* Skills and Tools of an Effective Investigator
Who
more...
Recruiting is Critical to Your Success What is the Secret - Webinar By GlobalCompliancePanel
...ch site to conduct their studies.
Areas Covered in the Session:
* How to set up and track your recruiting of subjects
* The challenges of successful recruiting
* The importance of your recruiting staff in the overall success of the unit or site
* How to build a data-base of patients
* How to recruit more efficiently for a target study
* Factors involved in
more...
Understanding the Calibration Curve - Webinar By GlobalCompliancePanel
...help to eliminate these problems.
Areas Covered in the Session:
* Calibration Basics
* Types of Calibration - External standard, Internal standard, etc.
* Calibration Options - Response factor methods, Linear regression
* Evaluation of Data - Three tools for evaluating regression data
* Discussion using real-world data sets
Who Will Benefit:
* Method
more...
Project Management for Clinical Trials - Webinar By GlobalCompliancePanel
...ing to use electric data capture.
Areas Covered in the Session:
* What is a Project and why is it important for running clinical trials?
o Defining the key characteristics of project management and the importance to clinical trials
o Using an project management process for improving the success of your own clinical trials
* Setting clear objectives and
more...
Meet FDA Expectations for a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
...n. Coping with "rogue" suppliers.
Areas Covered in the Session:
* Regulatory "Hot Buttons"
* Classify suppliers; Supplier requirements by "classification"
* What's behind the COA? The COC?
* The FDA's increasing emphasis on the site audit
* Types of remote audits
* Maintaining the relationship
Who Will Benefit:
* Senior management in Drugs, Devices,
more...
Developing and Using the Product Risk Management FileReport - Webinar By GlobalCompliancePanel
...intain it as a "living document".
Areas Covered in the Session:
* The Revised ISO 14971: 2007 for Devices
* ICH Q9 for Pharma
* Product Hazard Analysis
* Design, Process, and Use[r] Failure Mode, Effects and Criticality Analysis
* Fault Tree Analysis
* Suggested Risk Management File / Report, FMECA, FTA Templates
* The Team and Its Involvement - Who, When
more...
Change Control -- Your Companys GMP Weak Point - Webinar By GlobalCompliancePanel
...nagement buy-in. Supplier buy-in.
Areas Covered in the Session:
* Change Control a what it is; what it is not
* Areas impacted by Change Control
* Regulatory / FDA 483 a Hot Buttonsa
* Design Control
* Document Control
* Identifying changes
* Preventing negative changes
* Maintain a 'state of control'
* Business needs and obtaining 'buy-in'
more...
Tougher US FDA cGMP Compliance Audits - When Youre Not Ready - Webinar by GlobalCompliancePanel
...nown deficiencies for FDA review.
Areas Covered in the Session:
* 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'
*
more...
Introduction to Investment Risk - Credit Market and Portfolio - Webinar by GlobalCompliancePanel
...works and standards in use today.
Areas Covered in the Session:
PART ONE - Market Risk
After attending this session, you will be able to:
* Differentiate between Qualitative and Quantitative Techniques
* Apply Three Approaches to Value at Risk (VaR)
* Understand the Limitations of VaR
* Prepare for Black Swans
PART TWO - Volatility, Risk Aversion, and Portfolio
more...
From Guru - Your Online Mentor
Information Security - Overview


Information security means 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
more...
From GlobalCompliancePanel
Excel Spreadsheets and FDA Device Regulations - Webinar by GlobalCompliancePanel
...ems that are will be hard to fix.
Areas Covered in the Session:
* Overview of the regulations
o Automated processes
o Production and process changes
o General record keeping requirements
o Electronic records
* Excel Validation
o Setting the validation criteria
+ Data types
+ Using lists to
more...
Process Validation current industry practices and FDA Guidance Document Review - Webinar by GlobalCompliancePanel
... of process validation protocols.
Areas Covered in the Session:
* Recent Guidance Documents
* Industry Practices
* Examples of Process Validation Protocols
* What should be included in Process Validation Protocols
* The Importance of Good Process Validation
* Common mistakes in Process Validation
Who Will Benefit:
* Director of Quality
* Manager
more...
Understanding the Technical Requirements of 21 CFR Part 11 - Webinar by GlobalCompliancePanel
...tations of the regulation if not properly addressed. This session will provide a focus on understanding the key considerations for the technical 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
more...
International Financial Reporting Standards The Basics - Webinar by GlobalCompliancePanel
...these changes mean for companies.
Areas Covered in the Session:
* GAAP vs. IFRS
* What will change
* What will not change
* Who needs to comply
* The four key principles of IFRS
* How disclosure requirements will change
* The new rules for assigning values to assets
* The deadlines for adoption
* How IFRS will affect SOX compliance
* How
more...
Reprocessing REUSABLE Medical Devices-Cleaning Labeling Requirements - Webinar By GlobalCompliancePanel
Overview: Much attention has been paid to the regulatory requirements of reprocessing SINGLE use devices.
However, there is increasing attention being directed towards reprocessing REUSABLE medical devices and regulatory requirements. The purpose of this seminar is to explain the rationale, the legal requirements and some methods commonly used for reprocessing & validating reusable medical
more...
Food Safety Management Systems - ISO 220002005 - Webinar By GlobalCompliancePanel
...ndard for Food Safety Management.
Areas Covered in the Session: The following areas will be addressed:
* Key terms and definitions
* General Requirements
* Documentation
* Management Responsibility
* Resource Management
* Planning and Realization of Safe Products a flow diagrams, process steps and control measures
* Hazard Assessment - Control Measures
more...
Controlled Substances and the Pharmacist - Webinar By GlobalCompliancePanel
...ilities placed on the pharmacist.
Areas Covered in the Session:
* Discuss the types of federal criminal and civil actions that can be imposed on a pharmacy pertaining to the purchase, sale, transfer, dispensing, destruction and theft or loss of Schedules II through V controlled substances.
* Identify the responsibilities of DEA through their Diversion personnel to enforce federal
more...
Hazard Analysis vs FMECA Differences and Commonalities - Webinar By GlobalCompliancePanel
...lopment phases will be discussed.
Areas Covered in the Session:
* Hazard analysis techniques
* FMECA techniques
* Probabilistic approaches
* When to use which method during the design process
* Effective evaluation strategies and documentation formats
Who Will Benefit:
* Project Managers
* Regulatory Affairs
* System Engineers
* R&D
*
more...
Labeling Requirements for Dietary Supplements - Webinar By GlobalCompliancePanel
Overview: This webinar points out current labeling issues including misbranding that are eating into profitability of dietary companies.
The webinar teaches the attendee how to avoid common labeling compliance issues including:
* Misbranding
* Misleading claims
* Misleading statements
* Directions of use
The webinar focuses on general labeling provisions for dietary
more...
Medical Device Changes and The 510k - Webinar By GlobalCompliancePanel
...umented and defensible rationale.
Areas Covered in the Session:
* FDA Device Clearance / Changes in Direction
* Product Changes and Filing a New 510(k) Responsibilities
* Tracking / Evaluating Changes and the "Tipping Point"
* "Risk-Based"
* FDA's K97-1 and "Decision Tree" Model / Matrix
* Resolving a "Wrong" Decision
Who Will Benefit:
* Senior
more...
Validating Excel and Word Applications Documents - Webinar By GlobalCompliancePanel
...ce 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
* Realistic Limits of Apps Software V&V
* Suggested Approaches
* How to Implement, Execute and Document
more...
Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel
...to prove "progress against plan".
Areas Covered in the Session:
* Why formal Project Management
* The three most common tools
* How to compile
* Gantt, CPM, PERT
* Simple construction techniques
* Work breakdown Structure, Milestones, Tasks
* Effectiveness - Determining and Monitoring
* The "New Product Example"
* The "Remediation Example"
more...
Effective Training Practices for FDA Compliance - Webinar By GlobalCompliancePanel
...rmance, it must be done properly.
Areas Covered in the Session:
* Review of GMP regulatory expectations of training (FDA and EU)
* Recent training-related citations
* High-Level description of a training system, including elements (needs analysis through evaluation), basic training documentation, management, GMP training plans/ planning, and trainers
Who Will Benefit:
more...
Legal Risks in Social Media for Healthcare Providers - Webinar By GlobalCompliancePanel
...a social media marketing program.
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
*
more...
Preparing for GFSI and other Third Party Audits - Webinar By GlobalCompliancePanel
... organization are the keys to a successful audit.
This session will allow your team to anticipate the auditors needs and result in the facility'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
more...
Chemical Control for Food Manufacturers Ingredient Cleaning and Hazardous Materials - Webinar By GlobalCompliancePanel
Overview: A comprehensive review of an ideal chemical control program will be presented.
The guidelines presented will enable your company to implement programs that are cost effective and meet or exceed the expectations of major QSR, and GFSI audit criteria. This presentation will provide not only a provide schematic for management and control of chemicals, but an interactive and customizable
more...
Why is CAPA so often cited in medical device inspections - Webinar By GlobalCompliancePanel
... to be reviewed by investigators.
Areas Covered in the Session:
* Review CAPA citations in FDA-483 and Warning Letters
* Identify common problems with CAPA
* Identify FDA CAPA regulatory requirements
* Identify ISO 13485 CAPA requirements
* Explore FDA's risk expectations of CAPA systems
* Establishing a risk-based CAPA system
Who Will Benefit:
*
more...
Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations - Webinar By GlobalCompliancePanel
... CAPA and Change Control Systems.
Areas Covered in the Session:
* What should be investigated - Complaints, audit observations, deviations, discrepancies, calibration out-of-tolerances
* FDA expectations for investigations
* The investigation-problem resolution process - understand the problem, identify possible causes, data collection, data analysis, root cause
more...
Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel
...d to miss this important webinar!
Areas Covered in the Session:
* Why water myths develop
o Impact of c-GMPs
o Well-meaning but misguided precedents
o Scientifically unchallenged traditions and benchmarking
o Rule-hungry culture
* Water System Microbial Control Myths
o WFI from RO
o Turbulent Flow and Flow Rate
more...
Electronic Raw Data in Regulated Environments - Definition Recording and Archiving - Webinar By GlobalCompliancePanel
...DA Record Retention and Retrieval
Areas Covered in the Session:
* FDA Requirements for raw data and meta data
* FDA Inspection and enforcement practices
* Recommendations from industry task forces: GAMP/ ISPE guides
* Definition of raw data: original records vs. standard electronic formats, paper print-outs
* Ensure and demonstrate integrity of raw data
* The
more...
Medical Device Reporting Regulations and Violations - Webinar By GlobalCompliancePanel
...nufacturers for these violations.
Areas Covered in the Session:
* Review the FDA's Medical Device Reporting requirements.
* Review FDA 483 MDR Reporting issues
* Review Warning Letter Medical Device Reporting citations
* Establish common problems in MDR reporting
* What should MDR procedure contain?
* What actions should be taken by complaint personnel?
*
more...
Internal Audits Maintaining your Quality Systems at the Ready - Webinar By GlobalCompliancePanel
Overview: While not captured in most audit reports, one of the biggest mistakes an organization can make is to have insufficient self audits.
Internal audits are a core component of the Quality Assurance and Food Safety program. Ensuring the team representatives are trained and calibrated is a critical aspect of the program. An untrained team will miss important audit items, compromising the
more...
Operational Risk Management Ensuring Safety for Food Systems - Webinar By GlobalCompliancePanel
...eration - risk management simply requires attention. This session will establish a way of thinking about risks and their management that allows managers to simply define and incorporate risk reduction strategies into their own processes. Emphasis is on defining and managing risk levels prior to problems that may lead to significant setbacks. The procedures covered are mathematically sound,
more...
Analytical Instrument and Equipment Qualification in Quality Laboratories - Webinar By GlobalCompliancePanel
...d external regulatory inspectors?
Areas Covered in the Session:
* Regulatory requirements for analytical instrument qualification
* Calibration and Metrology Programs
* USP
* ICH Q2
* GXP
* Equipment and Instruments - similarities and differences
Who Will Benefit: This webinar will provide valuable assistance to all regulated companies that need to
more...
How to Prepare and Submit a Bullet Proof 510k and Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanel
...ehalf of their company in this open-forum and interactive session
Who will benefit: This course is appropriate to those involved in all aspects of the premarket notification, i. e., 510(k) process on behalf of medical device and In Vitro Diagnostic manufacturers. It is both a primer for personnel new to the FDA 510(k) process, or an excellent refresher course for those who need to revisit
more...
Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine
... and maintaining them in the DHR?
Areas Covered in the Session:
* FDA Quality Systems Regulation Requirements/ Definitions
* MDD Requirements/ Definitions
* Design History File (DHF)
o Definition
o Typical contents
o DHF and outsourced design/ production
o DHF and OEM relationships
* Device Master Record (DMR)
o
more...
Excel Spreadsheets - Develop and Validate to Eliminate 483s - Webinar By GlobalCompliancePanel
...features, and data entry verification.
What makes this session unique is the combination of step-by-step instructions and the hands on workings of each participant. Bring your laptop and use Excel for your own needs. This session will make you a better Excel user, saving you time and costs.
Areas Covered in the Session:
* Become compliance when using Excel spreadsheets for GxP
more...
Key Concepts in Successful Water System Sanitization - Webinar By GlobalCompliancePanel
... process for better optimization.
Areas Covered in the Session:
* Understand the basic water system sanitization concepts
* Use this understanding to design effective microbial control measures for your water systems
* Use this understanding to solve microbial problems originating from poor sanitization practices
* Debunk a few water system myths related to sanitization
more...
Preventive and Corrective Maintenance Protect your assets Protect your consumers - Webinar By GlobalCompliancePanel
Overview: A how to guide to meeting customer expectations of the maintenance function.
An overview of industry best practices and a review of some leading software solutions.
Why you should attend: Maintenance is often found to present the greatest area of opportunity for improvement in the food safety chain. Lack of control of parts and condition of equipment often contributes foreign
more...
Medical Device Tracking Latest FDA Update and Expectations - Webinar By GlobalCompliancePanel
...pporting device used outside a device user facility. This session will address the latest FDA guidance requirements and expectations and expound on why tracking methods must provide certain critical information about the location of a tracked device. Plus, FDA understands that manufacturers will have different tracking methods and procedures.
Areas Covered In the Session:
* Review the
more...
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant - Webinar By GlobalCompliancePane
...a study. Forewarned is forearmed.
Areas Covered in the Session:
* How to know when the protocol is not followed (PNF)?
* What is the difference between a protocol deviation and a violation?
* Importance of the "Protocol" in the number of deviations occurring
* How to ensure that the protocol will be followed exactly?
* What is in the Regs about following the
more...
Statistical Sampling Plans for Audits - Webinar By GlobalCompliancePanel
Overview: The purpose of auditing is to identify failures in the system or gross negligence.
The real question, "how bad does the system need to be for auditing to work?" This talk will look at statistical distribution for rare events to show that the sample size needs to larger when the systems are better. This is a paradox for most auditors who when a problem is discovered increase their
more...
Recalls Removals and Market Corrections in Compliance with FDA and ISO Requirements - Webinar By GlobalCompliancePanel
...pany's inability to ship product.
Areas Covered in the Session:
* Regulatory definitions of recalls, removals, and market corrections
* Instances which require recalls, removals, or market corrections
* What to do during recalls, removals, and market corrections
* Recordkeeping requirements for recalls, removals, and market corrections
* ISO 13485-specific
more...
FDA 483 Observations in the Laboratory What went wrong How can they be avoided - Webinar By GlobalCompliancePanel
...bservation on other laboratories.
Areas Covered in the Session:
* Regulations
* Inspectional Guidances
* Laboratory controls
* Specification, standards, sampling plans, test procedures
* Conformance to specifications
* Complete data
* OOS
* Following procedures
Who will benefit: The following individuals and disciplines will benefit from this
more...
101 cGMP To-Do List for 2011 - Webinar By GlobalCompliancePanel
...-have's for corporate compliance.
Areas Covered in the Session:
* Mandated Areas for Annual Reviews
* The Master Validation Plan -- Corporate and Site(s)
* Training Issues
* CAPA
* Trending
* Facilities; Production and Process Controls
* Suppliers, Contract Employees, Consultants
* Some basic OSHA Concerns; ties to the cGMPs
* Adverse Events
more...
A Comparison of ICH Q-10 Quality System and the FDAs Quality Systems Approach QSA to the Pharmaceutical GMPs - Webinar By Global
...e between compliance and quality.
Areas Covered In the Session:
* What are the objectives of ICH-Q10 and the FDA's Quality Systems Approach to Pharmaceutical Good Manufacturing Practices?
* What are the similarities and differences between these guidance documents?
* What are some Pro and Cons of the product lifecycle for pharmaceuticals
* Is the Quality Systems
more...
Basics of OTC Drug Labeling Compliance - Webinar By GlobalCompliancePanel
...ug labeling will also be covered.
Areas Covered in the Session:
* OTC Drug Labeling regulations: background and requirements
* Drug Facts labeling
* OTC Monographs and their importance
* Conditions under which OTC Drugs can be marketed in the U. S.A.
Who Will Benefit: Anyone who wants to market OTC drugs in the U. S.A. and assure that they're labeled properly with
more...
Introduction to Operational Risk - Webinar By GlobalCompliancePanel
...sk.
Areas Covered In the Seminar: After attending this session, you will be able to:
PART ONE
* Identify the major categories of Risk according to Basel
* List the seven major categories, 20 categories, and 40 subcategories of operational risk
* What to look for in taking a holistic and systematic approach to op risk
* Comprehend the major qualitative and
more...
Complaint Handling in Compliance with FDA and ISO Regulations - Webinar by GlobalCompliancePanel
...session will include the requirements for defining, documenting, and implementing a complaint-handling system, including the requirements for complaint review, investigation, and corrective action, as well as the ISO-specific implications.
This session will discuss the best way to document customer feedback, what constitutes a complaint, and what do with "non-complaint" feedback. Also
more...
Training Requirements and Practices to Assure QSR and ISO Compliance - Webinar by GlobalCompliancePanel
...ee training program must be in place to assure this. This session will instruct attendees on the regulatory requirements of personnel training, and establishment of a training program, including new employee training, methods of training, how to document training so that it is readily available for review (by managers, auditors or inspectors), when to evaluate training requirements, training
more...
How to Prevent Food Safety Problems Using Your Current Quality System - Webinar by GlobalCompliancePanel
Most industries have become reasonably sophisticated in terms of applying the principals and tools involved in quality control and improvement.
Unfortunately, food supply chain members have lived outside of the quality world and have not invested the time, training or money to learn and apply the disciplines needed to bring quality into preventive levels of control. Visual inspection in many
more...
The ICF Process Tips on Achieving Optimal compliance and Comprehension - Webinar by GlobalCompliancePanel
The ICF process, which involves communication between a consentee (patient/ subject) and a consenter (staff clinician/ designee), is a vital component to the authorization of any medical intervention or clinical research trial.
IRBs, sponsors and clinical sites all share the responsibility of ensuring an adequate ICF process. Any inadequate ICF training to clinical sites and /or unclear
more...
Excel Spreadsheet Validation To Eliminate 483s - Webinar by GlobalCompliancePanel
This interactive webinar provides explicit details and live demonstration followed by a collaborative workshop that explains how to configure and validate a GxP compliant spreadsheet application.
What makes this session unique is the combination of step-by-step instructions and the hands on workings of each participant. Bring your laptop and use Excel for your own needs. This session will make
more...
Developing an Effective Supplier and Internal Auditing System - Webinar by GlobalCompliancePanel
The FDA regulations contain a vast quantity of requirements, which govern tasks performed by your company's personnel every day.
Are there going to be noncompliance? You bet. Are you going to correct these noncompliances? Only if you identify them. To ensure substantial compliance, your company needs an effective audit program for both internal and external processes. To have an effective audit
more...
Best Practices in Complaint Management - Compliance Webinar by GlobalCompliancePanel
... the most frequently cited observations on FDA-483s. This session will include the requirements for defining, documenting, and implementing a complaint-handling system, including the requirements for complaint review, investigation, and corrective action, as well as the ISO-specific implications. This session will discuss the best way to document customer feedback, what constitutes a complaint,
more...
From Student Shelter In Computers ®
Student Shelter In Computers EC-Council Academic Partner Offers Certified Ethical Hacker CEH Course













...ering
Module 10: Denial of Service
Module 11: Session Hijacking
Module 12: Hijacking Webservers
Module 13: Hacking Web Applications
Module 14: SQL Injection
Module 15: Hacking Wireless Networks
Module 16: Evading IDS, Firewalls, and Honeypots
Module 17: Buffer Overflow
Module 18: Cryptography
Module 19: Penetration Testing
For More
more...
From Lodestone Digital
Adobe eLearning Suite



Lodestone Digital provides public Adobe eLearning Suite classes across the country that are certified by Adobe.
In addition to our public classes, we can provide Adobe eLearning Suite training at your location for students who need custom solutions. Our instructors have years of Adobe eLearning Suite production experience, and specialize in implementing digital media tools into a workflow.
more...
From A2ZJava
Advanced Java JSPs and Servlets Short Term


...tion Parameters - ServletConfig and ServletContext
* Session Management - using cookies as well as URL Rewriting
* Attributes vs Parameters
* JSP action tags - jsp: useBean, jsp: setProperty and jsp: getProperty
* RequestDispatcher - forward and include
* jsp: forward and jsp: include
* jsp: include vs include directive
* Error Page forwarding via JSP
*
more...
From ProfessionalOrganizers . com
Excel at Filing - On-Demand Webinar
The computer is an excellent organizing tool and yet the last thing clients want to do is buy more software. In this popular webinar, Certified Professional Organizer ® Debra Milne takes you through the different ways Microsoft Excel ® can be used to create an electronic filing system including electronic filing practices; printing file inventory lists; searching and tracking files;
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From Mohd Arsalan
Online Excel Macros VBA Training -Get it from Home
Learn writing excel macros and master the vba skills at the comfort of your home. Using online screen sharing mode with a systematical training plan acquire the necessary macro skills to automate your day-2-day excel activities. The training will give a competitive advantage to you over your colleagues. The training will be for 10 hours divided as per your interest.
Payment can be done after
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From TaxLiens.com
Wholesaling Houses for Monster Profits
Learn how to make serious money fast with real estate, buying and selling properties without ever even owning them with expert instruction from Sharon Restrepo during this special 90-minute online educational training session. Wholesaling real estate is quickly emerging as one of the hottest investing options in today's market because it is risk-free and it has the potential to be an enormous cash
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From Strategic Agile Technologies
Complete Java Training
...tend the classes with next batch if you miss any training sessions.
* 2 months of free technical support will be provided after training*
===========================
Core Java basics.
* History and Overview
o Structured Programming
o Object-Oriented Programming
* Java Basics
o Java Introduction
o Hello Java Program
o Compiling and Interpreting Applications
o JDK API
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From Design By DesAnn
Staging In The ZONE 5 week Webinar Series
...corded for you to view at your leisure if you miss a live session.
Week One-Staging in the Zone Fundamentals
Learn the decorating fundamentals that will help the process of decorating to sell. Staging in the Zone, is a DSA proprietary process that divides the room into horizontal layers to better establish balance of weight, lines, and color. See how to increase the visual footprint of a
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From Fire Tech Productions, Inc
NICET Water Based System Layout Level I CBT Webinar Series





This Level I NICET Water-Based Systems Layout webinar series is the best exam prep around! Learn the information, tips and techniques needed to pass the exam from Industry Leaders with over 50 years experience. This package contains 2 1. 5 hour LIVE sessions, online course access for 90 days, recorded versions of each session and our Level I Basic Water Based Systems Layout Reference Text.
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NICET Fire Alarm Level I CBT Webinar Seires
Two 2 hour sessions and 90 day access to your online training accountand recorded versions of each session. For those students who learn best with instruction, our Webinar courses provide live, NICET certified instructors to guide you through your study. Simulated exams finalize this course for maximum preparation!
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From Total Medical Compliance
Basics of Fraud Abuse Complimentary Webinar
... and abuse compliance requirements.
At the end of the session each learner will be able to:
Define Fraud and Abuse a it is not always intentional.
Recognize pertinent federal and state laws related to fraud and abuse a intentional or not.
Explain the importance of a Compliance Plan and how to determine the effectiveness of the plan.
The time is now to reduce your chances of an
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From Avant Resources
Using Social Networking Sites and Search Engines to Screen Applicants
...session will focus on strategies for getting what you need while minimizing potential complaints for discrimination or invasion of privacy.
During this 90 minute webinar you will learn:
a The legal limits of a social media policy
a What are the risks in using these sites?
a Isna t everything on the web fair game since privacy is waived once someone places something on the
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From Traders Mentoring Academy
Futures Trading Fundamentals Course
The Futures Trading Fundamentals Course has been designed for traders seeking to gain a strong foundation in the trading of the most popular financial and equity index futures. This is a concise course which focuses on the fundamental aspects of futures such as inter-market analysis and figures trading. This is not a replacement for our full mentoring course but is a companion to it for traders
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From PsyAsia International
Online Basic Psychometric Course

This is a very basic introductory course for those interested in psychometric tests at work. If you are looking for a qualification in psychometrics. This course runs over 5 weekly sessions, starting at 5. 45pm on Wednesdays. Each session lasts for 40 minutes and there is time after this for questions and discussion. The course is subsidised by PsyAsia, but there is a small fee of just US$3. 50
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From Pravam Pte Ltd
MM - SRM Workshop - An Online Preview on Jan 22nd 2010


Starts: Saturday January 22, 2011, 02: 00PM SGT
Ends: Saturday January 22, 2011, 03: 00PM SGT
Event Type: Other
Location: This is a virtual event.
Price:
Website: http://www. pravam. com
Industry: pharmaceuticals
Keywords:
Intended For: IT Managers, Procurement Managers, SAP Consultants, SAP MM End Users, SAP Project Managers, SAP Manager, SAP Training Manager/ HR Manager
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From EmBusTech Software Solutions Pvt Ltd
SAP APO DP SNP PPDS GATP SNC
...nd Planning module
We will start with a basic session, providing a supply chain overview and where do various modules (Demand Planning, Supply Network Planning, Production
Planning and Detailed Scheduling, Transportation Vehicle & Scheduling and Global Available to Promise) of APO fit in the big picture of Supply Chain. We will
also give you a flavour of various topics that
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From SiteSell
SBI eLearning July 6 2010 at 7 PM EDT






Our most popular class date is back for a new, 12-week session. Come join your Instructor and fellow classmates to build your business in a fun, friendly and effective atmosphere.
In addition to your live online review sessions, you have videos and tools to use between sessions so that your business building progress is rapid!
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From PsyAsia International
Chinese Personality at Work
This is a FREE webinar in PsyAsia's HRM themed webinar series. In this session we are pleased to present research on and answer questions about whether or not Chinese people are significantly different to other major groups and whether any potential differences are likely to impact upon the ability of personality tests to predict performance at work.
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From TrainHr
Conflict Management and Dealing with Difficult People - Webinar By Trainhr
This session is designed to help you manage more effectively by understanding the reasons for conflicts and giving you ways to diffuse negative employees to get desired results and increased productivity and teamwork
more...
Management Styles that Work Best for Each of the Four Generations in the Workplace - Webinar By Trainhr
This session is designed to help you manage more effectively by being able to differentiate between each generation and adapt to their style and outlook and capitalize on their strengths
more...
The Truth About Pay for Performance Techniques for Difficult Economic Times - Webinar By TrainHR
...session will also discuss uncommon strategies that can have a greater impact on performance and morale than traditional pay for performance systems. Key strategies for non-profit organizations will also be discussed as there are compensation techniques that can be employed in any environment. A good compensation system is designed with clear goals, communicated clearly, and executed flawlessly.
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From Business901
Marketing Your Black Belt
...
Program Structure and Agenda: During the first three sessions you will receive all the tools and training needed to design your individual 28-day marketing action plan. You will signed up to start on the 2nd Thursday and for the following 28 days. There is a limited number of seats.
Session 1: 60 minutes(Friday@ 11: 00AM)
Session 2: 60 minutes(Monday@ 11: 00AM)
Session 3: 60
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From International Contact Center Academy
Attracting Retaining Engaging the Next-Generation Workforce The Being of Soul-Inspiring Leadership
...her youa re an emerging or established leader, this session is for you. That is, if you are ready to deepen learning and take action on embodying the practices of soul-inspiring leadership. You may or may not have direct reports, but are in a position of influence a responsible for getting your results with and through others.
The main a requirementa is a strong commitment to
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Contact Centre Group 2010 Webinars Lean Six Sigma Demystified Practical Easy to Implement Ideas A Handy Guide for Managers Su
...ts on agent interactions.
Why will attendees find this session valuable?
Innovative process re-engineering programs like Lean Six Sigma have heightened the ability of organizations to successfully capitalize on the value of the company's assets in significant ways. Yet, in the midst of all these performance improvement programs and initiatives most managers agree that the single greatest
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From Nurture Talent Academy
Bootstrapping in a Social Venture - Experience Sharing session by an Ashoka Fellow
In a startup social enterprise, passion is often the sole driver. A social entrepreneur does not attract investors very easily because they are often looking for a quick buck, barring a few benevolent funding agencies. So the only way out for a social entrepreneur is to bootstrap for a long time, before some agency like Ashoka, recognizes their efforts and lends support. But the idea of
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How to Build Communities in the Social Media and Energize Your Customers Towards Your Brand While Achieving Business Objectives
All social media channels have their own USP. Given the need of the hour almost all of us have an account in most of these most popular social media websites. Several of us create communities, join others' communities, answer to posts, create posts, etc. But do we always do all such activities to achieve the purpose that took us there. Do we always strategize our moves in the social media? If the
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From Obiee Online Training
Obiee Online training Interactive
...nfidence. I will also give you a video of my own recorded session of a real obiee interview. This will help you how to answer in the interview.
I will give you OBIEE job support if you get any issues in the real time.
Will give you complete OBIEE material for your reference which nobody will have in general.
You can cancel the course with in first 2
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From iT corner
High School Algebra Overview
A course that offers a general review of High School Algebra topics in preparation for College admissions and GED tests.
This course is perfect for individuals who need a refresher of basic and intermediate Algebra topics.
This course is 80 hours long and it is divided in sessions lasting from 2 to 4 hours per session. The duration of the sessions can be discussed in order to accomodate to
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From Nurture Talent Academy
Effective use Of Social Media For Entrepreneurs
Every day millions of people are using social networking and creating social media content. Originally viewed as simply entertainment for teenagers, nowadays social networking is the fastest growing way for companies to:
* market their products and services
* engage their customers
* generate more leads and shorten the sales cycle
* expand their brand
This session on "Social
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Opportunities of Starting a healthcare venture
...ooking for Quality care at affordable prices. In today's session we will listen to an expert medical entrepreneur Anil Hebbar, speaking about the opportunities galore.
Speaker
Anil, is the founder cum managing director of Emergent Medi-tech India Pvt Ltd. Anil has worked in a few highly responsible positions across a number of of engineering and product development companies in various
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From 4MAT 4Business
Free Online Course 4MAT 8-Steps to Design
The Secret to Learning: The Four Questions That Must Be Answered
The secret to engaging instructional design and delivery: all learning includes the asking and answering of four questions. These questions form a cycle of learning. This four-part cycle applies to learning anything. You followed this cycle when you learned to ride a bike, when you learned that second language in high school and
more...
Inform 10 Activity Frameworks for Increasing Interactivity in Lecture
Who should attend: Instructional Designers and Trainers
In Step 4, Inform, the trainer shares the information the learner must know to generate the desired learning outcomes. This is typically where the trainer lectures. However, lecture isna t all talk. How do we make lecture interactive and engaging? In this session, we will explore 10 structures for increasing interactivity. Structures
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Too Much Information Too Little Time How to Conceptualize Content
Who should attend: Instructional Designers
When: April 19, 2011 at 2 pm Central
You are tasked with sharing an enormous amount of information in a short period of time. In this session, we will explore strategies for increasing retention and engagement. You will explore how to define a concept for your courses and practice conceptualizing content using movies and real-world content.
more...
Trainers Toolkit Inventory of Training Tools and Techniques for Dynamic Delivery in all Four Parts of the Learning Cycle
Who should attend: Instructional Designers and Trainers
There are four parts to the 4MAT Learning Cycle: Engage, Share, Practice and Perform. In this session, you will explore easy-to-apply concrete tools and techniques for guiding the learning process. Youa ll see examples of how these tools can be used in live and online training with any content.
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From Scientiabio
Online LIVE training in Bioinformatics and Clinical Research




... will be getting complete theoretical as well as hands on session in the related software.
3. You can comfortably choose your time for the training every day as per your convenience.
4. Entire training program is LIVE, so at any point of training you can always communicate with the trainer.
5. All you need to have a desktop computer or laptop with internet connection.
6. Training fees is
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From Global BioPharmaceutical Resources, Inc. (GBPR, Inc.)
21 CFR Part 11 the details of what it means
This webinar takes the requirements of Part 11 and details them into specific things to do in all three primary areas: SOPs, product features, and validation. It describes what to do to be compliant thereby avoiding 483s and warning letters. All required IT SOPs are covered. All industry standards product features are discussed. The 10-step risk-based validation approach is outlined so that the
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From PC Smartz
Excel 2007 - Getting Started
This class highlights the basic introduction to Excel 2007. This session is 90 minutes of online, live instructor-led training customized to meet the individualized needs of the group. Learn how to navigate a spreadsheet, enter/ edit data, add formulas and some time saving shortcuts. Classes are limited to 10 students. See our website for more information at www. pcsmartz. com.
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From Staging and Redesign
Creating an E-Newsletter
...s make when sending newsletters
This is a "don't miss" session!
Hear what other stagers thought about Marro's seminar:
"Already an admirer, I decided to try Melissa's newsletter program. She laid it out so beautifully and logically in posts here that I just followed the template. Why bother to reinvent the wheel? Works for her, why not try it here for me?
The rest is history. My
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From Keen Info Solution
SAP ABAP Online Training ECC 60
...ets
* BDC Programming
* Call Transaction
* Session Methods
13 LSMW
* Over view of LSMW
* Creation of Project , Sub Project , Object Type
* Creation of Batch Input Using Recording Mode
* Steps To Create LSMW
14 Module Pools
* Over view of Module pools
* Creation of Create button
* Creation of Display
* Creation of Sub
more...
Online Training for SAP ABAP ECC 60 with 6y Real Time Expert
...ad
* Data sets
* BDC Programming
* Call Transaction
* Session Methods
13 LSMW
* Over view of LSMW
* Creation of Project , Sub Project , Object Type
* Creation of Batch Input Using Recording Mode
* Steps To Create LSMW
14 Module Pools
* Over view of Module pools
* Creation of Create button
* Creation of Display
* Creation of Sub screens
* Creation of Tab Strip
* Creation
more...
Online Training for Oracle CRM R12 with 6y Real Time Expert
Course : ORA-CRM Duration: 30 w. days
Faculty : Classes : 2hrs
ORACLE CUSTOMER RELATIONSHIP MANAGEMENT (CRM)
CRM Application Foundation
a Overview of CRM Application Foundation integration
more...
Online Training for Oracle RAC DBA with 6y Real Time Expert
...Impact in RAC
Wait events and wait events views
Session and system statistics
Database locks
AWR snapshots & reports in RAC
ADDM analysis
Day 4:
Unit-8
Oracle Clusterware Administration & Diagnosing
What is oracle clusterware
Oracle clusterware registry
Voting disk
VIP Address
Maintenance of Clusterware log files
Cluster
more...
Online Training for Oracle SCM R12 with 6y Real Time Expert
...unts, Adjustments, and Approvals
Topics Covered During Session
Overview of Oracle E-Business Suit process
ORACLE AIM (Application Implementation Methodology)
Overview of Documentations in Real-time Projects
Over view of other Service Oriented modules Integrations
ORACLE ORDER MANAGEMENT
Order to Cash Lifecycle
Ordering and Scheduling Process
Pricing Process
Shipping Process
more...
From Global BioPharmaceutical Resources, Inc. (GBPR, Inc.)
Excel Spreadsheet Validation-Step by step guide to complianc
This interactive webinar explains how to configure and validate a GxP compliant spreadsheet application to avoid FDA 483s. It has a detailed presentation and live Excel demonstration followed by an interactive workshop. What makes this session unique is the combination of step-by-step instructions and the hands on workings of each participant. Bring your laptop and use Excel for your own needs.
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From PsyAsia International
Online Psychometric Test Administration Training
...the essentials of psychometric test administration over 3 sessions. Each session lasts 65-90 minutes, meaning that in total there is approximately 4 hours of material to view. The material is recorded from a recent series of LIVE training sessions in test administration. Enrolled students will be able to view the slides and trainer presentation/ narrative (in English). Additionally you will
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From Consult SCM
SAP APO Supply Network Planning

...uled based on the convenience of participants.
* All sessions are interactive and questions are encouraged during the session itself to gain maximum benefit out of the training.
* Assistance in preparation for Certification exam
* Help in preparation for Job interviews and placements
Please contact training@consultscm. com or call at following US numbers 312-912-9722 /
more...
SAP APO Demand Planning

...nsult SCM (www. consultscm. com) is conducting a training session on APO Demand Planning module starting in 3rd week of March, 2010 for a duration of 8 sessions in total spanning across next few days. The entire training module would be divided into following sub-modules for logical flow of training.
1. Basic SAP APO overview
2. Basic SAP Business Intelligence
more...
From ABJADE Consulting
online mobile learning training session
...session
There is an online m-learning training session next week .The training sessions is entitled "Introduction to the use of Mobile Learning in corporate for training and professional support". Mobile Learning is using handheld
devices and cell phones for providing customized training and learning. This
can be used through a special mobile learning system provided by ABJAD.
more...
From Silva Life Success Coaching
The Silva Life System Live Video Interactive Learning Seminar
...e than 8-10 people.
For your convenience, we offer two session times:
Saturday's 9: 00 AM -12: 00 PM and Saturday's 1: 00 PM - 4: 00 PM
Starting November January 9, 16, 23 , & January 30
The Silva Method equips you with the tools you need to evaluate your productivity...increase your creativity...supercharge your problem-solving capability...and greatly exceed your goals!
more...
From Business Expert Webinars
Secrets to Delivering Presentations That Win Business
...e to implement the teachings from this eLearning training session.
Kristina Schwende has over 25 years experience in both the private and public sectors. She is a graduate of the esteemed Protocol School of Washington where she received her certification as a Corporate Etiquette and International Protocol Consultant. She also received her training certification through Peak Potentials
more...
How to Become A Great Sales Leader
...hip planner to help you implement the teachings from this session.
Walter W. Hoff is President of Development First, LLC, a leadership development company that provides consulting, facilitation, and design services to clients in various industries focused on building the skills of present and future leaders of people.
Walt has more than 29 years of corporate experience, the last 25 in the
more...
The Busy Professional's Guide to Social Networking
...ing Simple' to help you implement the teachings from this session.
Lynne Jarman-Johnson is a dynamic business owner who helps businesses and non profits with communication planning and implementation. Companies feeling overwhelmed and stressed over budgets, employee morale, team ineffectiveness turn to Lynne for guidance and invigoration. Marketing/sales/advertising teams that work against
more...
Secrets to Delivering Presentations That Win Business
...e to implement the teachings from this eLearning training session.
Kristina Schwende has over 25 years experience in both the private and public sectors. She is a graduate of the esteemed Protocol School of Washington where she received her certification as a Corporate Etiquette and International Protocol Consultant. She also received her training certification through Peak Potentials
more...
Influencing Anyone and Everyone
Whether we want to influence our management, negotiate with vendors, or create partnerships with other department or company leaders, we need to know how build trust and form strong partnerships that are a win-win situation for both parties.
This session will cover:
Understanding different communications styles
Understanding how people want to receive information
Understanding the
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Motivating the Underachieving Employee
...tively set the tone for the meeting so it is a productive session with the employee
Soften the impact of tough questions so the employee responds openly and does not become defensive
Solicit input from the employee for an active conversation
Get the employee to take ownership of action steps and follow through on them
Use the three most critical phrases when concluding the meeting
As an
more...
Guerilla Team Leading
There are many books written about leading teams. Teams are so important today because they utilize the individual talents that are brought together to accomplish complicated projects that no one person could accomplish by themselves. This presentation gives you the top most important keys to leading a team to becoming high-performing.
The session will cover:
The power of teams
Assigning
more...
Accountability versus Blame
... this sound like you? If not, then be sure to attend this session. Do your employees have the motivation to achieve what you want?
Does achievement make difference in the success of the team and do you and your employees know how to recognize that difference? Can other members of the tem tell e when an employee has achieved or not achieved? Do your employees know that they have to achieve or
more...
Secrets to Delivering Presentations That Win Business
...e to implement the teachings from this eLearning training session.
Kristina Schwende has over 25 years experience in both the private and public sectors. She is a graduate of the esteemed Protocol School of Washington where she received her certification as a Corporate Etiquette and International Protocol Consultant. She also received her training certification through Peak Potentials
more...
Secrets to Delivering Presentations That Win Business
...e to implement the teachings from this eLearning training session.
Kristina Schwende has over 25 years experience in both the private and public sectors. She is a graduate of the esteemed Protocol School of Washington where she received her certification as a Corporate Etiquette and International Protocol Consultant. She also received her training certification through Peak Potentials
more...
Let Me Think It Over. I'll Get Back to You...Now what?!
...s the QUALITY of the numbers that is most important. This session will teach sales professionals and business owners alike the importance of knowing what those numbers are. What are the specific steps each salesperson must achieve to make a sale? How do you shorten the 'sales cycle'?
What two questions you should NEVER ask your prospects.
A specific frequency of follow-up contacts that
more...
Too busy for you? Learn 5 quick techniques to benefit your health picture.
It is hard for the busy professional to know what to eat to maintain a healthy lifestyle. The choices you make today at your business luncheon and dinner sales meeting impact your mood, metabolism and mental clarity.
In this webinar, you will learn practical tips on how to know what food is suitable for consumption, and how to implement these tips into your busy day from renowned Wellness
more...
How to Become A Great Sales Leader
...hip planner to help you implement the teachings from this session.
Walter W. Hoff is President of Development First, LLC, a leadership development company that provides consulting, facilitation, and design services to clients in various industries focused on building the skills of present and future leaders of people.
Walt has more than 29 years of corporate experience, the last 25 in the
more...
From MicroType
FrameMaker-to-PDF Advanced Techniques
...sessions, December 2+3)
(B) Enhanced interactivity and automation (2 sessions, December 7+9)
(C) Testing PDFs (1 session, December 10)
For experienced users of FrameMaker and Acrobat who want to create/ maintain high-quality, interactive Acrobat PDF files.
Parts A, B and C can be taken as a complete course or separately.
Price:
(A) = US$300;
(C) = US$150;
(B) = US$450,
more...
From Business Expert Webinars
Become An Effective Solution Sales Person
...n from which prospects love to buy.
You will leave this session being able to
Differentiate yourself from your competition using reverse engineering strategies
Create value with prospects so they only want to buy from you
Build relationship based on trust, not price
Compose questions for a powerful needs analysis discussion with your prospects
All registrants receive
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Migrating from a Product Sales Person to a Solution Sales Person
...son from which prospects love to buy. You will leave this session being able to
Differentiate yourself from your competition using reverse engineering strategies
Create value with prospects so they only want to buy from you
Build relationship based on trust, not price
Compose questions for a powerful needs analysis discussion with your prospects
All registrants receive
more...
Leveraging LinkedIn to Grow Your Business
... some examples or collaboration using LinkedIn.
In this session you will:
Create Lead Generation Strategies that work
Accelerate your Sales opportunities by leveraging LinkedIn.
Understand how to take advantage of this social network to grow your business.
Learn how to make your on line profile work to attract business.
Discover how LinkedIn can work to grow your business.
Gain a fresh
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Powerful Follow-up Techniques That Drive Prospects to Buy
Sales Tactics to Unclog Your Sales Funnel
Low closing ratios on outstanding proposals is one of the biggest issues plaguing sales organizations large and small. Most salespeople simply don't know how often to contact prospects, or what to do or say when they do contact them. They end up doing the same things their competitors do, with increased pressure to reduce price to close sales.
David
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