6-Hour Virtual Seminar

6-Hour Virtual Seminar on GCP/GLP/GMP : Comparison and Understanding of the FDA’s 3 Major Regulations

John E Lincoln Instructor:
John E Lincoln 
6 Hours
Webinar ID: 501867

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Price Details
Recorded Webinar
$595 One Attendee
$945 Corporate Recorded

Recorded: Access recorded version, only for one participant unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)

Corporate Recorded: Access recorded version, Any number of participants unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)


The Good Laboratory Practice regulations describe the minimal standards for conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for products regulated by FDA or EPA such as animal food additives, human and animal drugs, medical devices for human use, biological products, electronic products, or pesticide products.

The Good Clinical Practices regulations pertain to studies utilizing human subjects or clinical studies. While the GLPs do not specifically pertain to basic exploratory studies carried out to determine whether a test article has any potential utility or, for FDA studies only, to determine the physical or chemical characteristics of a test article, adherence to their principles will further ensure the accuracy of any results achieved. And the GMPs pertain to the manufacture of products to be used in trials and then in release to the field/public.

Why should you Attend:
This seminar will define what are the US FDA's expectations for proper laboratory / clinical / manufacturing practices, systems, equipment usage, and documentation / record-keeping. It will evaluate the requirements for how basic Quality Management System (QMS) expectations/requirements are addressed in this environment.

The seminar with evaluate pharma GMPs and 21 CFR 58 and associated regulations to see how the GLPs can be implemented in the real world to achieve FDA requirements and ensure the accuracy and repeatability/reproducibility of lab results. There will be a detailed analysis of the applicable regulations for the industry. Subject areas considered are:

  • Lab / Clinical / Manufacturing Control / Systems
  • Facilities and Equipment
  • Documentation and Records
  • Materials Management
  • Personnel / Assignments
  • Validation
  • The Lab GLPs, IRBs/GCPs, and company CGMPs

  • Key Regulatory Expectations
  • GLP/ GCP / GMP specifics
  • Systems, Personnel, Facilities
  • Required documentation/records
  • Control of equipment/test material/samples
  • Laboratory Controls in the CGMPs
  • Clinical documents
  • CGMP requirements
  • Validations

Who Will Benefit:
  • Senior management in Devices, Pharma, and Combination Products
  • QA / RA
  • Medical Products Development and Testing Teams
  • R&D
  • Engineering
  • Production
  • Operations
  • Marketing
  • Consultants; others tasked with Medical Product Development, Manufacturing, Logistics, and V&V Responsibilities

Speaker Profile
John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and described in peer-reviewed technical articles, and workshops, world wide.

John has also managed pilot production, regulatory affairs, product development/design control, 510(k) submissions, risk management per ISO 14971, and projects; with over 28 years of experience in the FDA-regulated medical products industry - working with start-ups to Fortune 100 companies, including Abbott Laboratories, Hospira, Tyco/Mallinckrodt. He is a graduate of UCLA.

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