GMP for Quality Control and Contract Laboratories 2016

  • 30 Nov 2016
  • Hilton Zurich Airport, Switzerland

Description

Topics
  • Company`s quality plan or laboratory compliance master plan
  • The regulatory background and GMP requirements for quality control and contract laboratories
  • How to develop inspection ready documentation
  • The difference between GMP and non-GMP laboratories
  • How to avoid and/or respond to the FDA inspectional observations and warning letters
  • GMP requirements
Who should Attend

Attendees from:

  • QA managers and personnel
  • Analysts and lab managers
  • Regulatory affairs
  • Validation specialists
  • Human resources (HR) managers and staff
  • IT professionals
  • Documentation department
  • Training departments
  • Consultants& teachers

Past Events

Important

Please, check "GMP for Quality Control and Contract Laboratories" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Hospitals & Clinics
Science: Laboratories

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