Complying with 21CFR Part 11-Understanding the Role of Predicate Rules

Instructor: Tony Dunbar
Product ID: 700177
  • Duration: 60 Min
AN overview of the Part 11 regulation, with special emphasis on the key role played by the applicable predicate rules as the starting point for any Part 11 compliance assessment.


In spite of the FDA’s clarification regarding the scope of electronic records subject to Part 11 as expressed in the Sep 2003 Guidance for Industry, much discussion and debate still surround the topic.

recorded version

1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Mar-2008

Training CD / USB Drive

One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367


Read Frequently Asked Questions

Why Should You Attend:

Many individuals still seem to miss the key fact that Part 11 only applies to records called for by predicate rule, maintained in electronic form and used in that form for regulated activities. This presentation will give a general overview of the Part 11 regulation itself, with special emphasis on the key role played by the applicable predicate rules as the starting point for any Part 11 compliance assessment. This will be illustrated by practical examples from the pharmaceutical and medical device industries.

Areas Covered in the seminar:

  • Part 11: Brief history and background
  • Did GMPs change with Part 11?
  • Validation and Part 11
  • What is a predicate rule?
  • Examples of predicate rule records
  • Examples of predicate rule signatures
  • Risk based approach to Part 11
  • Future of Part 11

Who Will Benefit:

This seminar will provide valuable assistance to all regulated companies subject to FDA 21 CFR Part 11, including companies in the Pharmaceutical, Medical Device, Diagnostic and Biologics fields. The employees who will benefit include:

  • Validation specialists
  • QA managers and personnel
  • Information Technology managers and personnel
  • Regulatory affairs
  • Consultants
  • Quality system auditors

Instructor Profile:

Tony Dunbar, M.Sc., has over 25 years experience in Quality Management with Warner-Lambert/Pfizer and currently with PENSA as their Senior Compliance Consulting Expert. PENSA ( provide compliance services and validation/compliance software to the Life Science Industries. In his role at PENSA, Tony has performed, on behalf of a number of industry-leading clients, assessments and validation of various computer systems against Part 11 requirements. These systems have included ERP, LIMS, HPLCs, etc. Tony has also been a presenter of GMP topics and Part 11 at industry group seminars.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

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