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DTSTART:19700308T020000
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UID:2140535:Event:470856
DTSTAMP:20260905T114814Z
SUMMARY:Introduction to Medical Device Quality System Regulations
DESCRIPTION:In this webinar, you will get an overview of FDA’s medic
 al device Quality System Regulation, 21 CFR Part 820.\nWhy Should You 
 Attend:\nYou will learn FDA’s expectations for the implementation an
 d on-going operation of an effective medical device quality system.\nF
 DA’s medical device Quality System Regulation, 21 CFR Part 820 , i
 ncludes requirements related to the methods used in, and the facilitie
 s and controls used for, designing, manufacturing, packaging, labeling
 , storing, installing, and servicing of medical devices intended for h
 uman use. This webinar will address these matters.\n\nAreas Covered in
  the Webinar:\n\nRegulatory basis\nQuality System\nDesign Controls\nDo
 cument Controls\nPurchasing Controls\nIdentification & Traceability\nP
 roduction & Process Controls\nAcceptance Activities\nNon-conforming Pr
 oduct\nCorrective & Preventive Action\n\nWho Will Benefit:\nMedical de
 vice company personnel working in production, R&D, regulatory affairs,
  QA, and QC.\n\nFor more information visit https://medtechiq.ning.com/
 events/introduction-to-medical-device-quality-system-regulations
DTSTART;TZID=America/New_York:20211208T100000
DTEND;TZID=America/New_York:20211208T130000
CATEGORIES:webinar
LOCATION:online
WEBSITE:https://www.complianceonline.com/medical-device-quality-system
 -regulations-webinar-training-706648-prdw?channel=MedTech%20I.Q
URL:https://www.complianceonline.com/medical-device-quality-system-reg
 ulations-webinar-training-706648-prdw?channel=MedTech%20I.Q
CONTACT:8887172436
ORGANIZER;CN=ComplianceOnline:https://medtechiq.ning.com/profile/Refer
 ral512
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/9855363273?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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