New FDA or EMA and USP Guidelines for Transfer of Analytical Methods 2017

  • 18 May 2017
  • Webinar

Description

New FDA or EMA and USP Guidelines for Transfer of Analytical Methods 2017 is a webinar that covers topics such as:

  • Examples of FDA warning letters and how to avoid them
  • FDA and International expectations for method transfer
  • Comparative testing according to the new FDA method validation guidance
  • The FDA Guidance on method transfer: examples for type and extent of testing
  • Gap analysis according to the new EU GMP chapter 6 on method transfer
  • The USP chapter (1224): history, status, future
  • Responsibilities of the transferring and receiving laboratory
  • Four approaches for analytical method transfer and testing
  • Criteria and approaches for risk based testing: what, when, how much?
  • Developing a transfer plan and a pre-approval protocol
  • Method transfer from standard HPLC to UHPLC
  • Selecting parameters and acceptance criteria for comparative testing
  • Handling deviations from documented acceptance criteria
  • Most likely failures during method transfer
  • Method transfer protocol and summary report
  • Justification and criteria for transfer waiver (omission of formal transfer)

New FDA or EMA and USP Guidelines for Transfer of Analytical Methods 2017 is intended for:

  • Lab Supervisors and Managers
  • Analysts
  • Consultants
  • QA Managers and Personnel
  • Teachers

Past Events

Important

Please, check "New FDA or EMA and USP Guidelines for Transfer of Analytical Methods" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical laboratories, Medical technology

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