2014 - China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
Topics/Call fo Papers
Biotechnology
Other CFPs
- 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
- Role and Responsibilities of the HIPAA Compliance Officer
Last modified: 2014-02-19 13:52:17