FDA Medical Device Approval Process (510(k), IDE, PMA) 2013

  • 12-13 Mar 2013
  • AAPS, North York, Canada

Description

The FDA Medical Device Approval Process is a course dedicated to FDA Medical Device Approval Process including:

  • Submission preparation and the underlying scientific
  • FDA device approval process
  • The structuring and assembly of 510(k)s
  • Regulatory principles involved
  • Amendments and supplements thereto
  • IDEs and PMAs
  • Post-approval documents

The FDA Medical Device Approval Process brings together attendees responsible for::

  • Research
  • Regulatory
  • Legal
  • Clinical
  • Quality
  • Manufacturing

Past Events

Important

Please, check "FDA Medical Device Approval Process (510(k), IDE, PMA)" official website for possible changes, before making any traveling arrangements

Event Categories

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

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