Introduction

This Process Validation Requirements webinar will review process validation basics, with emphasis on looking beyond compliance towards achieving a robust process. Review of process validation basics, with emphasis on looking beyond compliance towards achieving a robust process.

Area Covered In The Webinar

Global Harmonization Task Force requirements (includes FDA and ISO)

  • Installation Qualification (IQ)
  • Operational Qualification (OQ)
  • Performance Qualification (PQ)
  • Design Qualification
  • Facilities and utilities
  • Strategies for achieving a robust and reliable process.
  • Typical process validation protocols.

Why should you attend?

When used as intended, process validation can provide increased process reliability, improved yields, and reduced operating expenses.

Who Will Benefit

Managers, Supervisors, Directors, and Vice-Presidents in the areas of:

  • Research & Development
  • Quality Engineers and Auditors
  • Manufacturing Engineers Quality Assurance & Quality Control Teams
  • Operations Teams
  • Document Control
  • Device Development Teams
  • Personnel involved in Verification and Validation planning, execution and documentation for devices

ENROLLMENT OPTIONS

On Demand
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José Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device and life sciences industry specializing in man Know More

José Mora