Software Verification and Validation Planning and Documentation 2016 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 Verification and Validation Planning and Documentation 2016 is intended for:
- Engineering
- R&D
- Operations
- Production
- Consultants
