Software Validation for the New FDA Inspections 2013

  • 01-02 Jul 2013
  • The LaLit Mumbai, India

Description

Software Validation for the New FDA Inspections 2013 is a seminar that covers topics such as:

  • 21 CFR Part 11 - Compliance for Electronic Records and Signatures
  • Introduction to the FDA
  • The Five Keys to COTS Computer System Validation
  • HIPAA Compliance for Electronic Records
  • The Validation Team

Software Validation for the New FDA Inspections 2013 brings together QA, IT, Laboratory staff, QC, Regulatory Affairs, Managers, GMP, GCP and GLP professionals.

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Important

Please, check "Software Validation for the New FDA Inspections" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Pharma
Technology: Biotechnology, Information Technology (IT)

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