Software V&V Protocols and Documentation - Webinar By GlobalCompliancePanel 2012

  • 25 Jul 2012
  • Webinar

Description

Software V&V Protocols and Documentation is a webinar that covers topics such as:

  • The Project Validation Plan
  • Verification or Validation -- FDA Expectations
  • Product and Process / Test / Facilities / Equipment Software V&V
  • An FDA-accepted Documentation "Model"
  • GAMP / Other Considerations
  • When and How to Use DQ, IQ, OQ, PQ (or their equivalents)
  • "White Box" and "Black Box" Validations
  • The FDA`s 11 Key V&V Documentation Elements

Software V&V Protocols and Documentation brings together QA / RA, Senior management in Drugs, Devices, Biologics, Dietary Supplements, R&D, Software development, programming, documentation, testing teams, Production, Engineering, Consultants; others tasked with product, process, electronic records software V&V responsibilities and Operations.

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Event Categories

Education: Training
Health & Medicine: Healthcare, Medical device, Medical technology, Pharma

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