Draft Guidance for Device Industry and FDA - Postmarket Surveillance - Webinar By GlobalCompliancePanel 2011

  • 25 Oct 2011
  • Webinar

Description

Draft Guidance for Device Industry and FDA - Postmarket Surveillance is a webinar that covers topics such as:

  • The legal background and overview of statutory criteria
  • Review proposed changes
  • Expectations for postmarket surveillance study duration
  • Considerations regarding pediatric population provisions
  • Why an order for postmarket surveillance will issued under section 522
  • The postmarket surveillance process and identification of issue
  • The elements to Include in a Postmarket Surveillance Study Plan
  • Why postmarket surveillance study plans are reviewed as an original submission and its amendments until the plan is approved
  • Current expectations for different stages of Postmarket Surveillance Study Reports
  • Why FDA may order postmarket surveillance to address a wide variety of device-related public health questions
  • Why happens if you fail to complete a Postmarket Surveillance Study

Draft Guidance for Device Industry and FDA - Postmarket Surveillance brings together Clinical Affairs, Regulatory Affairs, Quality and Compliance, Investigators, Distributors/Authorized Representatives, Marketing & Sales, Consultants and Legal Counsel.

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Important

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Event Categories

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

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