Date :
Place : Switzerland, Zurich, switzerland
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 demonstratedDeadline for abstracts/proposals : 24th October 2017
Organized By :NetZealous DBA as GlobalCompliancePanel
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
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