Test Methods and Standards for Medical Device Design Verification and Validation 2016
14 Oct 2016
Webinar
Description
Topics
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
Who should Attend
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
Test Methods and Standards for Medical Device Design Verification and Validation 2016 - 14 Oct 2016, Webinar (62822)
Important
Please, check "Test Methods and Standards for Medical Device Design Verification and Validation" official website for possible changes, before making any traveling arrangements
