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Recorded Webinar

Virtual Seminar on Supplier Management in FDA-Regulated Industry

timelapse 3 Hrs with 10-15 Mins of Q and A

Note:

This webinar occured in the past
Along with recorded webinar, copy of presentation slides will be shared
Recorded Webinar can be played unlimited times

Speaker/Presenter

Short Abstract

Supplier qualification and assessment is required in both the QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend significantly less time and money, and still be in control of their suppliers and in compliance with the regulations. This seminar will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices. Also prominently covered will be supplier nonconformances: issuance, followup, and acceptance.

Areas Covered in the Webinar:

  • Supplier Qualification/Selection
  • Review of FDA requirements
  • Review of ISO requirements
  • Types of suppliers that must be qualified
  • Case Study: A Hypothetical Supplier Selection/Assessment
  • Use of Risk Assessment
  • Types of Supplier Nonconformances
  • Supplier Corrective Action Requests
  • Common Pitfalls


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