2-day In-person Seminar on Verification/Validation - Product, Process, Software and QMS at Las Vegas | Thursday, January 17th, 2013 | Las Vegas, United States

Contact Person : Event Coordinator; Last Date for the submission of abstract : 13/01/2013; Description : This course will review the company Master Validation Plan for major key inputs and CGMP deficiencies. It will address the FDA's newer and tougher regulatory stance.

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2-day In-person Seminar on Verification/Validation - Product, Process, Software and QMS at Las Vegas

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