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. Method validation recently got highest attention from regulatory agencies and industry task forces. For example, FDA and EMA released guidelines on method validation and transfer, and USP has

Date : 7th December 2017 to 8th December 2017

Place : Gambia The, Amsterdam

Website :https://www.eventbrite.com/e/validation-verification-and-transfer-of-analytical-methods-com-a-tickets-38837228195?aff=NDT

Contact Person:Paula Edwards

Description:

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. Method validation recently got highest attention from regulatory agencies and industry task forces. For example, FDA and EMA released guidelines on method validation and transfer, and USP has

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. Method validation recently got highest attention from regulatory agencies and industry task forces. For example, FDA and EMA released guidelines on method validation and transfer, and USP has will be held in Amsterdam,Gambia The on date 2017-12-08

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Deadline for abstracts/proposals : 6th December 2017

Keynote Speakers :

Conference Highlights :Learning Objectives: -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 -Understand the principles of validating methods developed in-house, verification of compendial methods, transfer of analytical procedures and demonstrat

Venue :Amsterdam, Netherlands

Check the event website for more details.