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2014 - Implementing a Medical Device Reporting (MDR) System Integrated with a UDI System
Topics/Call fo Papers
Biotechnology , Healthcare , Medical Device , Pharmaceutical
Other CFPs
- 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
- Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Configuration
- Implementing a Unique Device Identification (UDI) System - Issued on September 24, 2013
Last modified: 2014-02-19 13:52:48