DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements 2014

  • 14-15 Aug 2014
  • Hilton Grand Vacations Suites at the Flamingo, Las Vegas, NV, United States

Description

DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements 2014 is a seminar that covers topics such as:

  • The Design History File - documenting Product Design Control and its nine elements
  • The Design Control requirements of the CGMPs, 21 CFR 820.30
  • The EU’s Medical Device Directive
  • The Device Master Record and the Device History Record
  • The remaining elements of a Technical File / Design Dossier
  • The "Essential Requirements"; and their documentation
  • Two attendee projects
  • Trends

DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements 2014 is intended for:

  • Regulatory Affairs
  • Senior and middle management and staff
  • R&D
  • QA/QC
  • Manufacturing Engineers
  • Production Management
  • Project Managers
  • Process Engineers
  • Any tasked with medical device development, documentation, and regulatory responsibilities
  • Vendors, sales and marketing

Past Events

Important

Please, check "DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Healthcare, Medical device, Pharma
Technology: Biotechnology

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