Guidelines for New FDA Transfer of Analytical Methods – 2017

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


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. For a long time there was no official guidance on what exactly is expected to maintain ‘the validated state’.

Areas Covered in the Session:
Four approaches for analytical method transfer and testing
Responsibilities of the transferring and receiving laboratory
Developing a transfer plan and a pre-approval protocol

Who Will Benefit:
Lab Supervisors and Managers
QA Managers and Personnel

Speaker Profile:
Ludwig Huber Ph.D., is the director and editor of Labcompliance the global online resource for validation and compliance. He is the author of the books “Validation and Qualification in Analytical Laboratories” and “Validation of Computerized Analytical and Networked Systems, Informa Healthcare”.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

Ad Reference ID: 62158cfb7cbb9fbf

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