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DTSTART:19700308T020000
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UID:2140535:Event:56522
DTSTAMP:20260520T151536Z
SUMMARY:Process Verification and Validation Planning and Execution
DESCRIPTION:This 90-minute session on risk-based verification and vali
 dation planning will discuss \"must have\" elements from the U.S. FDA 
 cGMP, ICH Q9 and ISO 14971 for hazard analysis and product risk manage
 ment, and show how you can integrate these into a company's quality ma
 nagement system.\nWhy Should You Attend:\nFDA Warning Letters and rece
 nt high-profile recalls indicate major cGMP deficiencies in big name d
 evice and pharma companies. And now the FDA is taking an even tougher 
 stance. One major failing is lack of sufficient or targeted risk-based
  V&V planning. Why do companies need a Master Validation Plan? What ar
 e the must have elements from ISO 14971 and ICH Q9 for hazard analysis
  and product risk management? How can these be integrated into a compa
 ny's quality management system.\nThis webinar will help you develop or
  refine the company Master Validation Plan to meet FDA / cGMP expectat
 ions. It will address the FDA's newer and tougher regulatory stance.\n
  \n\nFor more information visit https://medtechiq.ning.com/events/pro
 cess-verification-and-validation-planning-and-execution
DTSTART;TZID=America/New_York:20120911T100000
DTEND;TZID=America/New_York:20120911T113000
CATEGORIES:medical, training
LOCATION:Online Event
WEBSITE:http://www.complianceonline.com/ecommerce/control/trainingFocu
 s/~product_id=701662?channel=MedtechIQ
URL:http://www.complianceonline.com/ecommerce/control/trainingFocus/~p
 roduct_id=701662?channel=MedtechIQ
CONTACT:+1-650-620-3915
ORGANIZER;CN=Referral:https://medtechiq.ning.com/profile/Referral
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562006613?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Referral:
 https://medtechiq.ning.com/profile/Referral
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