How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel 2011

  • 27 Apr 2011
  • Webinar

Description

The webinar will cover the following topics:

  • How to conduct a record audit
  • DHR audit
  • FDA warning letters
  • Major FDA 483 points and issuance prevention
  • QS regulation
  • Guidance documents

The event brings together:

  • Consultants
  • Regulatory and Compliance Managers
  • Operations executives
  • Directors, Managers and vice presidents
  • Quality assurance executives, engineers and field Auditors
  • Senior executives from pharmaceutical and medical device companies

Past Events

Important

Please, check "How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Operations, Quality assurance
Government & Global Issues: Law & Regulations
Health & Medicine: Hospitals & Clinics, Medical device, Pharma

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