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2014 - Design Change Analysis ? Four Considerations

Date2014-04-16

Deadline2014-04-16

Venueonline, USA - United States USA - United States

Keywords

Websitehttps://www.compliance2go.com/product/?p...

Topics/Call fo Papers

Medical Device

Other CFPs

  1. Transferring Medical Device Production to a Contract Manufacturer - Decision Making Process and Procedures
  2. Establishing an Internal Audit Program of the Quality Management Systems Pursuant to ISO 13485 and 21 CFR Part 820
  3. Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)
  4. FDA Recordkeeping Requirements
  5. Drug Master Files - Understanding and Meeting Your Global Regulatory and Processing Responsibilities

Last modified: 2014-02-19 13:47:36