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 : 25th October 2017 to 26th October 2017

Place : Switzerland, Zurich, switzerland

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901164SEMINAR?allconferencealerts-October-2017-SEO

Contact Person:Eevnt Manager

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 Zurich, switzerland,Switzerland on date 2017-10-26

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Deadline for abstracts/proposals : 24th October 2017

Keynote Speakers : 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. Presenter of the Year of the Institute for Validation and Technology Director and chief editor of www.labcompliance.com, the global on-line resource for validation and compliance issues for laboratories. Author of the books &

Conference Highlights :QA Managers and Personnel Quality Control Method Development Analytical Chemists Validation Specialists Laboratory Managers and Supervisors Regulatory Affairs Training Departments Documentation Departments Consultants

Venue : Zurich, Switzerland

Check the event website for more details.