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2014 - Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs

Date2014-06-24

Deadline2014-06-24

Venueonline, USA - United States USA - United States

Keywords

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

Topics/Call fo Papers

Medical Device

Other CFPs

  1. Establishing a Medical Device Complaint Handling System integrated with a UDI System
  2. 21 CFR Part 820 - Quality System Regulation -Applying Principles of Lean Documents and Lean Configuration
  3. Implementing a Medical Device Reporting (MDR) System Integrated with a UDI System
  4. China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
  5. US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus

Last modified: 2014-02-19 13:56:08