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UID:2140535:Event:63616
DTSTAMP:20260508T202516Z
SUMMARY:Building a Vendor Qualification Program for FDA Regulated Indu
 stries: One and Half Day In-Person Seminar
DESCRIPTION:Course Description:\nIf you are looking for the answer to 
 the following questions, you will certainly benefit from attending thi
 s seminar on building a vendor qualification program:\n\nHave you wast
 ed hours, days, and weeks on qualifying vendors that you know cannot o
 r will not meet your requirements?\nHas your approach to vendor qualif
 ication and vendor audits left you with internal CAPAs, customer audit
  items, or 483 observations?\nHave you wondered whether an onsite vend
 or audit is necessary in the eyes of FDA?\n\nWell, the answers to thes
 e and many more questions are now available in a simple to understand,
  yet detailed training session designed to help manufacturers of FDA r
 egulated products build (or rebuild) a sustainable vendor qualificatio
 n program.\n\nLearning Objectives:\nThis course on vendor qualificatio
 n program for FDA regulated industries will:\n\nDefine a sustainable s
 tructure for a vendor qualification program.\nExplain how change contr
 ol and other quality programs feed into the vendor qualification progr
 am.\nOffer usable audit forms/checklists and other vendor qualificatio
 n program document templates.\nExplain how to:\nDetermine the best pot
 ential vendor and what a potential vendor needs to supply before quali
 fication.\nInitially identify vendors that meet your requirements prio
 r to qualification.\nPerform on-site and off-site verifications.\nMoni
 tor and re-qualify vendors.\nEstimate costs and time associated with v
 endor qualification.\nRespond to customer and regulatory audit observa
 tions associated with vendor qualification.\n\n\nDiscuss common pitfal
 ls to avoid when qualifying vendors.\n\nWho Will Benefit:\nThis course
  will provide valuable assistance and guidance to all FDA regulated co
 mpanies for building sustainable vendor qualification program. The fol
 lowing job titles/ positions will benefit from attending this seminar:
 \n\nInternal Auditors\nRegulators\nLegal Departments\nCompliance Offic
 ers\nPurchasing Managers\nQC Managers\nQA Managers\nQuality and Sales 
 Department Staff\nCompliance Consultants\nSenior Management\n\n\nFor m
 ore information visit https://medtechiq.ning.com/events/building-a-ven
 dor-qualification-program-for-fda-regulated
DTSTART;TZID=America/New_York:20140320T083000
DTEND;TZID=America/New_York:20140321T130000
CATEGORIES:biotechnology, and, pharmaceutical
LOCATION:Courtyard Marriott Boston - Cambridge
WEBSITE:http://www.complianceonline.com/ecommerce/control/seminar?prod
 uct_id=80162SEM&?channel=medtechiq
URL:http://www.complianceonline.com/ecommerce/control/seminar?product_
 id=80162SEM&?channel=medtechiq
CONTACT:+1-650-620-3915
ORGANIZER;CN=ComplianceOnline:https://medtechiq.ning.com/profile/Refer
 ral512
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=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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