Test Methods and Standards for Medical Device Design Verification and Validation 2016

  • 14 Oct 2016
  • Webinar

Description

Test Methods and Standards for Medical Device Design Verification and Validation 2016 is a webinar that covers topics such as:

  • Design Traceability and risk management at all stages
  • Design verification and design validation activity cycles and maintenance throughout the product life cycle
  • Compatibility of the design with components and other accessories
  • Proof for how design outputs meet functional and operational requirements
  • Design outputs and documentation in DMR (Device Master Records) and DHR (Device History Records)
  • Test requirements to fulfill acceptance criteria for final products

Test Methods and Standards for Medical Device Design Verification and Validation 2016 is intended for:

  • Middle management
  • Senior management in medical device companies
  • Quality and manufacturing engineers
  • Research & Development
  • Quality Assurance & Quality Control Testing Personnel
  • Regulatory Affairs Professionals
  • Device Manufacturing Team
  • Device Design and Development Team
  • Verification and/or Validation planning and documentation teams for medical devices

Past Events

Important

Please, check "Test Methods and Standards for Medical Device Design Verification and Validation" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device

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