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2014 - Implementing a Unique Device Identification (UDI) System - Issued on September 24, 2013
Topics/Call fo Papers
Biotechnology , Healthcare , Medical Device , Pharmaceutical
Other CFPs
- Role and Responsibilities of the HIPAA Compliance Officer
- Design Change Analysis ? Four Considerations
- Transferring Medical Device Production to a Contract Manufacturer - Decision Making Process and Procedures
- Establishing an Internal Audit Program of the Quality Management Systems Pursuant to ISO 13485 and 21 CFR Part 820
- Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)
Last modified: 2014-02-19 13:48:47