Effective Design Controls in Accordance with Subpart C of 21 CFR, Part 820 2016

  • 22 Jan 2016
  • Webinar

Description

Topics
  • Clearly defining design inputs and outputs
  • Effective Design and development planning
  • Design verification versus design validation
  • The design review process
  • Design changes pre & post-design transfer
  • When does the design transfer
  • The Device Master Record (DMR)
  • Maintenance of the Design History File (DHF)
Who should Attend

Senior attendees involved or interested in:

  • Regulatory Professionals
  • Quality Professionals
  • Manufacturing Engineers
  • Design Engineers
  • Project Managers

Past Events

Important

Please, check "Effective Design Controls in Accordance with Subpart C of 21 CFR, Part 820" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance, Risk Management
Government & Global Issues: Law & Regulations
Science: Biochemistry, Life Sciences & Biology
Technology: Biotechnology

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