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DTSTART:19700308T020000
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UID:2140535:Event:470707
DTSTAMP:20260601T050223Z
SUMMARY:Building a Vendor Qualification Program for FDA Regulated Indu
 stries
DESCRIPTION:This course will provide detailed explanations and example
 s for Building a Vendor Qualification Program for FDA Regulated Indust
 ry. With today’s pharmaceutical market, raw materials, Active Pharma
 ceutical Ingredients (API), Containers & Closures, inactive or excipie
 nts and other components are being sourced from all over the world. We
  also have Third Party Manufacturers and outside testing facilities th
 at are part of our supply chains. Building and following a robust vend
 or qualification Program is essential for pharmaceutical and chemical 
 manufacturers. We must create a procedure, which will be used to remai
 n aware of the compliance status for all of our suppliers. Some raw ma
 terial components may move from producers to brokers to the end users.
  In addition, there may be other shippers and wholesalers responsible 
 for moving and holding our raw material components.\n\nLearning Object
 ives:\n\nThe laws that require supplier quality audits\nWriting robust
  procedures for a robust supplier quality audit program\nWho must cond
 uct these audits\nWhat are the qualifications needed for conducting su
 pplier audits\nHow much experience do auditors need\nWill experienced 
 auditors from another industry suffice for CGMP audits\nThe difficulti
 es of scheduling audits\nRequired number of days for each audit\nDo we
  have to cover every single operation during each and every audit\nFoc
 us on the more important audit objectives first\nWe will learn how to 
 adequately communicate our questions\n\nAreas Covered :\n\nThe qualifi
 cations of a supplier quality audit\nThe contents of an adequate suppl
 ier quality audit\nScheduling and planning audits\nRequired length of 
 audits\nEnsuring that all of our questions are adequately conveyed and
  understood by our suppliers\nHow to convince the suppliers that our a
 udits must be accepted and scheduled\nWhat do we do if the suppliers r
 equire us to pay a fee to audit them?\nDo we need secondary suppliers 
 for every component we use?\nLearning how to deal with the difficultie
 s of obtaining Travel Visas\nHow to maintain good conduct and respect 
 during audits\n\nWho will Benefit:\n\nQuality Assurance and Quality Co
 ntrols Managers, Supervisors and Directors\nSupply Chain Personnel\nSe
 nior Analysts in Chemistry and Microbiology and their Supervisors and 
 Directors\nResearch & Development Directors (for new products and supp
 liers\n\n\nFor more information visit https://medtechiq.ning.com/event
 s/building-a-vendor-qualification-program-for-fda-regulated-2
DTSTART;TZID=America/New_York:20211117T100000
DTEND;TZID=America/New_York:20211118T170000
CATEGORIES:seminae
LOCATION:online
WEBSITE:https://www.complianceonline.com/vendor-qualification-program-
 for-fda-regulated-industries-requirements-seminar-training-80162SEM-pr
 dsm?channel=MedTech%20I.Q
URL:https://www.complianceonline.com/vendor-qualification-program-for-
 fda-regulated-industries-requirements-seminar-training-80162SEM-prdsm?
 channel=MedTech%20I.Q
CONTACT:8887172436
ORGANIZER:Complianceonline
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/9746874854?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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