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2014 - How to Develop a Master Validation Plan

Date2014-03-11

Deadline2014-03-11

Venueonline, USA - United States USA - United States

Keywords

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

Topics/Call fo Papers

Biotechnology , Medical Device , Pharmaceutical

Other CFPs

  1. FDA 510(k) Update: Trends, New Strategy, Submission and FDA Clearance
  2. Harmonized Tariff Schedule Classification
  3. Ensuring 21 CFR 11 Compliance at Suppliers
  4. Training in Medical Device companies: Needs and effectiveness monitoring
  5. Demystifying an FDA-Compliant Medical Device Design Control, DHF, DHR, and DMR with a UDI System Integration

Last modified: 2014-02-19 13:33:39