PRV003 – Pharmaceutical Process Performance Qualification (PPQ) and Continued Process Verification (CPV)


2019

25

October

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Course Fee : $860
No HST

Duration : 1 Day

Time : 9 AM – 5 PM


This course will cover FDA approach on PPQ and CPV concept, rationale, writing protocols, reports and master validation plans, as well as the regulatory requirements of process validation that lead to risk-based, practical and scientific informed decisions and planned activities. It focuses on real work industrial scenarios. You will know how to initiate and conduct process validation studies in pharmaceutical and biopharmaceutical industries. You will also learn the related current process validation regulations and report writing for those validation studies.


Who should attend?

Production and Distribution

  • Production Manager
  • Formulator
  • Quality Control Analyst
  • Quality Assurance Associate

Research and Development (R&D), Analytical Development (AD)

  • Technician
  • Technologist
  • Analyst
  • Scientist

Validation

  • Validation Scientist
  • Validation Associate
  • Validation Engineer
  • Validation Assistant
  • Validation Coordinator
  • Technical Writer
  • Consultant
  • Scientist

25 Watline Ave, Suite #201, Mississauga, ON, L4Z 2Z1

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