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

Future Events

IQ, OQ, PQ in the Verification and Validation Process 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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