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2014 - Establishing an Internal Audit Program of the Quality Management Systems Pursuant to ISO 13485 and 21 CFR Part 820
Topics/Call fo Papers
Biotechnology , Medical Device , Pharmaceutical
Other CFPs
- Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)
- FDA Recordkeeping Requirements
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- 21CFR 11 Compliance for Excel Spreadsheet
- Conformance of Design History Files for Mature Medical Products
Last modified: 2014-02-19 13:46:26