IQ, OQ, PQ in the Verification and Validation Process

IQ, OQ, PQ in the Verification and Validation Process 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 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

Find Similar Events by Category

Education:   Training