Software Validation for the New FDA Inspections 2013

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

Description

Topics
  • 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
Who should Attend

QA, IT, Laboratory staff, QC, Regulatory Affairs, Managers, GMP, GCP and GLP professionals.

Past Events

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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