The following guideline can be ordered through the address listed in the "Source/Publisher"-category. In cases in which you can order through the Internet we have established a hyperlink.

FDA Guidance for Industry, FDA Staff, and October 4, 2004 FDA, regulated industry, and Division of Small Third Parties; Implementation of the third parties, Manufacturers, Inspection by Accredited Persons International and Program Under the Medical De



Document Type:
The purpose of the guideline is intend to implement new section of the act by accrediting third parties to conduct inspedctions of eligible manufacturers of Class II and III medical devices

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