ResearchBib Share Your Research, Maximize Your Social Impacts
Sign for Notice Everyday Sign up >> Login

Main Menu

Searching By

PARTNERS

Contact us

2014 - US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus

Date2014-04-29

Deadline2014-04-29

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. Anticipation and Expectations of a Medical OEM Design Control Audit
  2. Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Configuration
  3. Implementing a Unique Device Identification (UDI) System - Issued on September 24, 2013
  4. Role and Responsibilities of the HIPAA Compliance Officer
  5. Design Change Analysis ? Four Considerations

Last modified: 2014-02-19 13:51:40