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2014 - FDA Recordkeeping Requirements
Topics/Call fo Papers
Biotechnology , Medical Device , Pharmaceutical
Other CFPs
- Drug Master Files - Understanding and Meeting Your Global Regulatory and Processing Responsibilities
- 21CFR 11 Compliance for Excel Spreadsheet
- Conformance of Design History Files for Mature Medical Products
- Preparing for an FDA Inspection with Awareness - Dos and Don'ts
- Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
Last modified: 2014-02-19 13:45:04