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DTSTART:19700308T020000
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UID:2140535:Event:82316
DTSTAMP:20260523T195646Z
SUMMARY:Verification vs. Validation in Regulated Industries
DESCRIPTION:Overview\n\nThe meanings and regulatory requirements of th
 e terms \"verification\"and \"validation\"are often confusing to engin
 eers and even some regulatory professionals.\nOperations managers are 
 even less well versed. FDA regulations as well as European standards s
 uch as ISO 13485:2016 require both verification & validation documenta
 tion throughout these regulations and standards.\nThe terms apply to d
 esign control, process control and others. Numerous warning letters on
  this subject has been issued by FDA to well known manufacturers.\nVer
 ification and validation also appear in the \"essential requirements\"
 in MDD 93/42/EEC needed for CE marking medical devices in the European
  Union. Good engineering practices in all industries benefit from well
  executed verification and validation studies.\nThis presentation will
  define and explain the differences (& similarities) in these terms an
 d how they apply to regulated industries as well as the consequences o
 f poor adherence to these principles.\n\nFor more information visit ht
 tps://medtechiq.ning.com/events/verification-vs-validation-in-regulate
 d-industries
DTSTART;TZID=America/New_York:20190306T100000
DTEND;TZID=America/New_York:20190306T110000
CATEGORIES:webinar
LOCATION:Online evnt
WEBSITE:https://www.traininng.com/webinar/-200663live?channel=medtechi
 q-march_2019_SEO
URL:https://www.traininng.com/webinar/-200663live?channel=medtechiq-ma
 rch_2019_SEO
CONTACT:(510) 962-8903
ORGANIZER;CN="Joseph Wilcox":https://medtechiq.ning.com/profile/Joseph
 Wilcox
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/937471622?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Joseph W
 ilcox":https://medtechiq.ning.com/profile/JosephWilcox
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