Verification vs.Validation-Product,Process or Equipment and QMS Software 2018 is a webinar that covers topics such as:
- The Project V&V Plan
- Verification or Validation-FDA Expectations
- Product and Process/Test Facilities/Equipment Software V&V
- An FDA-accepted Documentation "Model"
- The FDA`s 11 Key V&V Documentation Elements
- When and How to Use DQ, IQ, OQ, PQ (or their equivalents)
- IEC 62304,GAMP/Other Considerations
- "White Box" and "Black Box" Validations
Verification vs.Validation-Product,Process or Equipment and QMS Software 2018 is intended for:
- QA / RA
- Senior management in Drugs,Devices,Combination Products,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
- Operations