Building a Vendor Qualification Program for FDA Regulated Industries: One and Half Day In-Person Seminar

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Dates : 20 March 2014 » 21 March 2014

Place : Boston, MA
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Course Description:

If you are looking for the answer to the following questions, you will certainly benefit from attending this seminar on building a vendor qualification program:

  • Have you wasted hours, days, and weeks on qualifying vendors that you know cannot or will not meet your requirements?
  • Has your approach to vendor qualification and vendor audits left you with internal CAPAs, customer audit items, or 483 observations?
  • Have you wondered whether an onsite vendor audit is necessary in the eyes of FDA?


Well, the answers to these and many more questions are now available in a simple to understand, yet detailed training session designed to help manufacturers of FDA regulated products build (or rebuild) a sustainable vendor qualification program


Learning Objectives:

This course on vendor qualification program for FDA regulated industries will:

  • Define a sustainable structure for a vendor qualification program.
  • Explain how change control and other quality programs feed into the vendor qualification program.
  • Offer usable audit forms/checklists and other vendor qualification program document templates.
  • Explain how to:
    • Determine the best potential vendor and what a potential vendor needs to supply before qualification.
    • Initially identify vendors that meet your requirements prior to qualification.
    • Perform on-site and off-site verifications.
    • Monitor and re-qualify vendors.
    • Estimate costs and time associated with vendor qualification.
    • Respond to customer and regulatory audit observations associated with vendor qualification.
  • Discuss common pitfalls to avoid when qualifying vendors.
Who Will Benefit:

This course will provide valuable assistance and guidance to all FDA regulated companies for building sustainable vendor qualification program. The following job titles/ positions will benefit from attending this seminar:

  • Internal Auditors
  • Regulators
  • Legal Departments
  • Compliance Officers
  • Purchasing Managers
  • QC Managers
  • QA Managers
  • Quality and Sales Department Staff
  • Compliance Consultants
  • Senior Management

Building a Vendor Qualification Program for FDA Regulated Industries: One and Half Day In-Person Seminar to be held in Boston, MA, 0 between 20 March 2014 and 21 March 2014. It covers specific areas of Biology and life sciences such as . Visit the website of the conference for more detailed information or contact the organizer for specific questions.
Add to calendar 2014-03-20 2014-03-21 Europe/London Building a Vendor Qualification Program for FDA Regulated Industries: One and Half Day In-Person Seminar https://www.sciencedz.net/en/conference/3924-building-a-vendor-qualification-program-for-fda-regulated-industries-one-and-half-day-in-person-seminar Boston, MA - 0

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