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DTSTART:19700308T020000
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UID:2140535:Event:64056
DTSTAMP:20260519T211727Z
SUMMARY:Best Practices in Supplier Management
DESCRIPTION:Overview:\nSupplier qualification and assessment is requir
 ed in both the QSR regulations and ISO standards.Many companies spend 
 a great deal of time and money in pursuit of compliance with this. Man
 y companies can spend MUCH LESS time and money, and still be in contro
 l of their suppliers and in compliance with the regulations. This pres
 entation will review the QSR and ISO requirements for supplier evaluat
 ion and assessment, and provide cost efficient, equally compliant opti
 ons to many of the most common practices. Areas Covered in the Sessio
 n:\n\nQSR and ISO 13485 requirements for supplier selection and assess
 ment \nHow to qualify new suppliers in a cost efficient manner\nHow t
 o assess current suppliers in a cost efficient manner\nHow to perform 
 supplier-related corrective action\nMinimum documentation requirements
  for supplier qualification, assessment, and related corrective action
 \n\nWho Will Benefit: This webinar will provide valuable assistance t
 o all regulated companies that are interested in incurring less cost o
 n supplier evaluation and assessment. The employees who will benefit i
 nclude:\n\nPurchasing management\nRegulatory management\nQA management
 \nConsultants\n\nCLICK HERE\n\nFor more information visit https://medt
 echiq.ning.com/events/best-practices-in-supplier-management
DTSTART;TZID=America/New_York:20140729T100000
DTEND;TZID=America/New_York:20140729T110000
CATEGORIES:seminar, pharma, medical, clinical, health, compliance, reg
 ulatory, fda
LOCATION:Online Event
WEBSITE:http://bit.ly/1lMoAvY
URL:http://bit.ly/1lMoAvY
CONTACT:18004479407
ORGANIZER:GlobalCompliancePanel
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562011671?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="John Rob
 inson":https://medtechiq.ning.com/profile/JohnRobinson
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