2014 - Drug Master Files - Understanding and Meeting Your Global Regulatory and Processing Responsibilities
Topics/Call fo Papers
Biotechnology , Pharmaceutical
Other CFPs
- 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
- Export to Mexico Documentation and Procedures
Last modified: 2014-02-19 13:43:35