Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should be demonstrated.

Date : 9th October 2017 to 10th October 2017

Place : United States, Burlingame

Website :https://www.eventbrite.com/e/validation-verification-and-transfer-of-analytical-methods-understanding-and-implementing-tickets-34482567287?aff=NDT

Contact Person:Paula Edwards

Description:

Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should be demonstrated.

Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should be demonstrated. will be held in Burlingame,United States on date 2017-10-10

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Deadline for abstracts/proposals : 3rd October 2017

Keynote Speakers : Dr. Ludwig Huber Chief Advisor - Global FDA compliance, Labcompliance Chairman, presenter and panel discussion member at US-FDA Industry Training sessions and conferences Served as 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 Systems. Director and chief editor of www.labcompliance.com, the global on-line resource for validation and compliance issues for laboratories.

Conference Highlights :Learn about the regulatory background and requirements for validation of analytical methods and procedures Learn how to plan, execute and document development and validation of methods developed in-house Be able to explain the different requirements for validation, verification and transfer of analytical procedures

Venue :Burlingame, CA 94010, United States

Check the event website for more details.