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2014 - Establishing a Medical Device Complaint Handling System integrated with a UDI System
Topics/Call fo Papers
Biotechnology , Healthcare , Medical Device , Pharmaceutical
Other CFPs
- 21 CFR Part 820 - Quality System Regulation -Applying Principles of Lean Documents and Lean Configuration
- Implementing a Medical Device Reporting (MDR) System Integrated with a UDI System
- China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
- US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus
- Anticipation and Expectations of a Medical OEM Design Control Audit
Last modified: 2014-02-19 13:54:48