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.
When
17 Jan 2013 @ 09:00 am
18 Jan 2013 @ 06:00 pm
Duration: 1 days, 9 hours
Where
Las Vegas
44726-44766 Aguila Terrace
Fremont
United States
Language
Englishen
Organised by
GlobalCompliancePanel (deactivated)
Event published: 12 Dec 2012 Event last updated: 18 Jul 2016