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2014 - 21 CFR Part 820 - Quality System Regulation -Applying Principles of Lean Documents and Lean Configuration

Date2014-05-21

Deadline2014-05-21

Venueonline, USA - United States USA - United States

Keywords

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

Topics/Call fo Papers

Medical Device

Other CFPs

  1. Implementing a Medical Device Reporting (MDR) System Integrated with a UDI System
  2. China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
  3. US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus
  4. Anticipation and Expectations of a Medical OEM Design Control Audit
  5. Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Configuration

Last modified: 2014-02-19 13:53:15