IQ, OQ, PQ in the Verification and Validation Process 2019 is a webinar that covers topics such as:
- The Master Validation Plan(s)
- IQ, OQ, and PQ, major components of robust Verification and Validation programs – Regulatory requirements
- Product Verification and Validation
- Individual V&V Plans and their execution
- QMS V&V and 21 CFR Part 11
- Process and Equipment V&V, including software
- Incorporating the Hazard Analysis / Risk Management tools of ISO 14971 or ICH Q9
- When / How to Use DQ, IQ, OQ, PQ
IQ, OQ, PQ in the Verification and Validation Process 2019 is intended for:
- Research and Development Departments
- Quality Assurance Departments
- Manufacturing Departments
- Regulatory Affairs Departments
- Operations Departments
- Engineering Departments
- Validation Departments
- Production Departments
- Documentation Departments
- Software Departments
- CGMP Instructors
- Consultants
