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2021 - Building a Vendor Qualification Program for FDA Regulated Industries

Date2021-11-17 - 2021-11-18


Venue, USA - United States USA - United States



Topics/Call fo Papers

The qualifications of a supplier quality audit
The contents of an adequate supplier quality audit
Scheduling and planning audits
Required length of audits
Ensuring that all of our questions are adequately conveyed and understood by our suppliers
How to convince the suppliers that our audits must be accepted and scheduled
What do we do if the suppliers require us to pay a fee to audit them?
Do we need secondary suppliers for every component we use?
Learning how to deal with the difficulties of obtaining Travel Visas
How to maintain good conduct and respect during audits
Follow-up on previous audit observations
The importance of learning the frequency and results previous Regulatory Audits
Questions and Answers from the audience

Last modified: 2021-10-18 23:22:46