2014 - Webinar On Design Verification, Validation and Testing for Medical Devices

. This webinar will educate you on the key areas that you need to focus on to fulfill the design control requirements for your medical device.
Areas Covered in the Session :
Product development process overview
Applicable design verification and validation requirements
Testing requirements including the pertinent ISO guidelines
Translation of user requirements into design inputs and role of testing and regulatory requirements
Fulfilling critical to customer and critical to quality requirements
Design verification and design validation activity cycles
Traceability and risk management at all stages
Design outputs and documentation in DMR (Device Master Records) and DHR (Device History Records)
Test requirements to fulfil acceptance criteria for final products
How to withstand regulatory scrutiny
How are changes and their effects controlled and documented during the device life cycle?
Summary
Who Will Benefit:
Senior management
Middle management
Research & Development
Quality Engineers
Manufacturing Engineers
Regulatory Affairs Professionals
Quality Assurance & Quality Control Personnel
Device Design Team
Device Development Team
Device Manufacturing Team
Verification and/or Validation planning, execution and documentation for devices.
Start up Company Leaders
For bookings and more information contact:
Compliance Trainings
5939 Candlebrook Ct,
Mississauga, ON L5V 2V5,
Canada
Customer Support : 416-915-4458
Email : support-AT-compliancetrainings.com