FDA`s New Enforcement of 21 CFR Part 11 - 2018

  • 20 Sep 2018
  • Webinar

Description

FDA`s New Enforcement of 21 CFR Part 11 - 2018 is a webinar that covers topics such as:

  • FDA`s new interpretation: learning from FDA inspection reports
  • FDA`s current inspection and enforcement practices
  • Justification and documentation for the FDA and your management
  • Strategy for cost-effective implementation of Part 11: A six step plan
  • Case studies how to avoid or respond to Part 11 related observations with corrective actions to fix current issues and preventive actions to prevent reoccurrence of the same or similar issues
  • Going through case studies from laboratories, offices and manufacturing with graphical workflow of records, step-by-step description, recommendations for individual Part 11 requirements with justifications and documentation for the FDA and your management
  • How to prepare your company for Part 11 Inspections

FDA`s New Enforcement of 21 CFR Part 11 - 2018 is intended for:

  • QA Managers and Personnel
  • QC Managers
  • Analysts
  • IT Administrators
  • Training Departments
  • Regulatory Affairs
  • Consultants
  • Documentation Department

Past Events

Important

Please, check "FDA`s New Enforcement of 21 CFR Part 11" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Pharma

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