Pharma Compliance: Upgrade Your Regulatory Training Program

Event Information
Product Format
Prerecorded Event
Conference Date
Tue, Jul 17, 2018
60 Minutes
Product Description

Train Beyond GMPs and “Read and Understand”

Regulatory agencies are putting increased scrutiny on your compliance training—and that means you are at risk if you’re not properly developing, implementing, and/or recording your employee education efforts. Of course, in addition to staying on regulators’ good side, providing well-organized, continuing compliance learning will yield a well-controlled operation and highly-competent workforce.

Join technical documentation consultant Charles H. Paul in this live webinar to learn exactly what types of compliance training you must offer and how to implement a training plan. Continuing compliance education is as important as any compliance discipline, Paul says, yet many training programs are improperly applied, poorly administered, and ineffectively managed. Don’t let that be said of your program. Paul will point you toward best-in-class training applications—and clue you into the key relationship between technical training and compliance documentation.

After attending this instructive session, you will know how compliance training affects employee performance—and which training applications are most appropriate for your organization’s circumstances. Whether you’re in the food, cosmetics, beverage, medical device, pharmaceutical, or biologics fields, you’ll know how to conduct a training needs analysis as specified by governing regulations. Learn how training should be applied, managed, and administered to cope with today’s regulated pharmaceutical industry!

Session Highlights
This program will teach you about:

  • Training in the context of compliance and regulated manufacturing
  • Training’s impact on employee performance
  • The types of training applications that are appropriate to specific circumstances
  • How a training needs analysis is conducted as specified by regulations
  • The training development process
  • Training beyond Good Manufacturing Practices (GMPs)
  • The relationship between technical training and compliance documentation
  • Training pitfalls and misapplications of training—and the impact on regulatory compliance
  • The dangers in relying on “Read and Understand”
  • How training should be managed in the modern pharmaceutical industry

Who Should Attend:

This webinar is applicable to professionals in the entire life sciences industry, and particularly in the pharmaceutical industry:

  • Operations managers and directors
  • Compliance managers and directors
  • Research and development personnel
  • Training managers and directors
  • Quality assurance managers and directors
  • Human Resources personnel

Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.


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About Our Speaker

Charles H. Paul

Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm. Charles is a management consultant, instructional designer and regulatory consultant and has led C. H. Paul Consulting, Inc. since its inception over 25 years ago. He regularly consults with Fortune 500 pharmaceutical, medical device, and biotechnology firms assisting them in achieving human resource, regulatory, and operational excellence....   More Info
More Events By The Speaker

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