How to Format Succinct and Comprehensive 510(k)s and PMAs 2012

  • 26-27 Apr 2012
  • Hilton Boston Park Plaza, MA, United States

Description

How to Format Succinct and Comprehensive 510(k)s and PMAs 2012 is a seminar that covers topics such as:

  • How to identify and assess the regulatory requirements
  • The recent changes in the 510(k) program and guidance documents relating to both 510(k)s and PMAs
  • How to increase a 510(k) and PMA submission quality
  • How to meet the regulatory requirements in a systematic, integrative manner
  • How to format succinct and comprehensive 510(k) and PMA submissions

How to Format Succinct and Comprehensive 510(k)s and PMAs 2012 brings together anyone in the FDA-regulated industry including, medical device, drugs, biologics, in vitro diagnostic devices or any combination products :

  • Clinical affairs (associates, specialists, coordinators, managers, directors and VPs)
  • Regulatory affairs (associates, specialists, managers, and directors)
  • Research and development (associates, scientists, managers, directors and VPs)
  • Quality assurance, quality control, and quality systems (associates, specialists, engineers, managers, directors and VPs)
  • Marketing (associates, specialists, managers, directors and VPs)
  • Product and development (associates, scientists, managers, directors and VPs)
  • Contract manufacturing organization (associates, scientists, managers, directors and VPs)
  • Site managers, and consultants
  • Senior and executive management (VPs, SVPs, Presidents and CEOs)
  • Contract research organization (associates, scientists, managers, directors and VPs)
  • Contractors and subcontractors

Past Events

Important

Please, check "How to Format Succinct and Comprehensive 510(k)s and PMAs" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Pharma
Science: Life Sciences & Biology

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