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