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2019 - A Bulletproof, Cost-Efficient Supplier Management Program
Date2019-06-14
Deadline2019-06-14
VenueOnline Event, USA - United States 
KeywordsMedical device supplier; Quality system regulation; ISO 13485 requirements
Topics/Call fo Papers
Supplier Selection
Review of FDA and ISO requirements
Types of suppliers that must be qualified
Defining critical suppliers
Classification of suppliers
Outsourced processes
The Quality Agreement
Recommended Practices
Supplier Assessment
Review of FDA and ISO requirements
Recommended Practices
How to avoid “Death by Supplier Audit”
Documentation requirements
Review of FDA and ISO requirements
Types of suppliers that must be qualified
Defining critical suppliers
Classification of suppliers
Outsourced processes
The Quality Agreement
Recommended Practices
Supplier Assessment
Review of FDA and ISO requirements
Recommended Practices
How to avoid “Death by Supplier Audit”
Documentation requirements
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Last modified: 2019-05-26 19:24:20