2-day In-person Seminar: Verification vs. Validation - Product Process Software and QMS

  • 1495.00 Dollar US$
  • Published date: May 17, 2016
  • Modified date: May 17, 2016
    • Las Vegas, NV, United States

Director : John E Lincoln

Seminar Link
http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900504SEMINAR?verification-vs-validation-qms-Las-Vegas

Course 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. This course's aim is to prove "Product Risk Based V&V" by sufficient, targeted and documented risk-based V&V test case elements/scripts. It will teach participants to evaluate its elements against ISO 14971 and ICH Q9 for hazard analysis and product risk management.

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