Managing Your FDA "483" Inspectional Observations 2017

  • 25 Oct 2017
  • Webinar

Description

Managing Your FDA "483" Inspectional Observations 2017 is a webinar that covers topics such as:

  • How to interpret the 483 - "How bad is it?"
  • What the 483 means
  • Responding to the FDA in writing
  • Managing the 483 discussion with the FDA at the conclusion of the inspection
  • What to expect during the next FDA inspection
  • Use of a Corrective and Preventive Action program

Managing Your FDA "483" Inspectional Observations 2017 is intended for:

  • FDA Consultants
  • Manufacturers
  • Regulatory Affairs Managers
  • Legal Counsel
  • Operations Directors
  • Quality Assurance Staff

Past Events

Important

Please, check "Managing Your FDA "483" Inspectional Observations" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Pharma

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