2014 - Preparing for an FDA Inspection with Awareness - Dos and Don'ts
Topics/Call fo Papers
Biotechnology , Medical Device , Pharmaceutical
Other CFPs
- Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
- Export to Mexico Documentation and Procedures
- Acceptance Sampling by Variables
- Acceptance Sampling by Variables
- Introduction to ISO 13485: Medical devices?Quality management systems?Requirements for regulatory purposes
Last modified: 2014-02-19 13:39:43