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, Sfo, ca

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901056SEMINAR?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 Sfo, ca,United States on date 2017-10-10

---

Deadline for abstracts/proposals : 7th 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. Presenter of the Year of the Institute for Validation and Technology Director and chief editor of www.labcompliance.com, the global on-line resource fo

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 :San Francisco Airport, San Francisco, CA, United States

Check the event website for more details.