Transfer of Analytical Methods According to the USP Chapter <1224>

Dr. Ludwig Huber

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This webinar will explain the final version of USP Chapter <1224> and FDA guidance for conducting and documenting method transfer between laboratories and sites, and provide tools for effective implementation.

Why Should You Attend:

When validated methods are transferred between laboratories and sites, their validated state should be maintained to ensure the same reliable results in the receiving laboratory. So far there has not been an official guidance on what exactly is expected to maintain 'the validated state'. This has changed since the USP has published the final version of the general chapter <1224>. Also the FDA has released an official guidance on how to conduct and document method transfer and FDA has been starting to enforce the new USP chapter. Now it is a good time to learn how to conduct and document method transfer.

This webinar will give a good understanding of USP and FDA requirements for transfer of analytical methods and provide recommendations and tools for effective implementation.

Free Hand-outs:

For easy implementation, attendees will receive

  • SOP: Transfer of Analytical Methods
  • Checklist: Transfer of Analytical Methods and Procedures
  • Master Plan template and examples: - Transfer of Analytical Methods and procedures

Areas covered in this webinar:

  • FDA and International expectations for method transfer.
  • Examples of FDA warning letters and how to avoid them.
  • The FDA Guidance on method transfer.
  • The new USP chapter <1224>: history, status, future.
  • Four approaches for analytical method transfer and testing.
  • Responsibilities of the transferring and receiving laboratory.
  • Developing a transfer plan and a pre-approval protocol.
  • Conducting comparative studies.
  • Criteria and approaches for risk based testing: what, when, how much?
  • The importance and selection of acceptance criteria.
  • Dealing with technology transfer: validation requirements, regulatory notification.
  • Method transfer from standard HPLC to UHPLC.
  • Most likely failures during method transfer.
  • Handling deviations from documented acceptance criteria.
  • Criteria for transfer waiver (omission of formal transfer).
  • Method transfer protocol and summary report.

Who Will Benefit:

  • Lab Supervisors and Managers
  • QA managers and personnel
  • GLP auditors
  • GLP study directors
  • Analysts
  • Consultants
  • Teachers
  • Pharmaceutical Research
  • Pharmaceutical development
  • Contract laboratories
  • CROs
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Training CD-USB

Physical CD-USB of recorded session will be despatched after 72 hrs on completion of payment

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Recorded video

Recorded video session

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Speaker: Dr. Ludwig Huber, Director and Chief Editor, LabCompliance

Dr. Ludwig Huber is Director and Chief Editor of www.labcompliance.com, the global on-line resource for validation and compliance issues for laboratories . Mr. Huber is an expert for FDA and equivalent international compliance and for ISO/IEC 17025 laboratory accreditation. He is also the Chairman, presenter and panel discussion member at US-FDA industry training sessions and conferences.

He served as a team member of PDA's task forces "21 CFR Part 11", of US-FDA internal documents, and of the GAMP® special interest group on laboratory equipment. In addition, he was awarded as Presenter of the Year of the Institute for Validation and Technology. He is the author of the books “Validation and Qualification in Analytical Laboratories, and "Validation of Computerized Analytical and Networked Systems", Interpharm Press.

For more information, visit www.ludwig-huber.com


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