2015 - Webinar on Design Verification, Validation and Testing for Medical Devices

Description :
Design Control is an integral part of any quality system in regulated industries. FDA Quality System regulation, Quality System Inspection Techniques (QSR and QSIT) and ISO 13485 have specific product verification and validation requirements that must be fulfilled in the medical device industry. FDA is getting more and more stringent about product design requirements for risk management and to fulfill its mandate for safety and efficacy of all medical devices. The design controls are now being expected from outside equipment manufacturers (OEM) and suppliers to the medical device industry. 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 at various phases of your product development.
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
Focusing on 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)
Proof for how design outputs meet functional and operational requirements
Compatibility of the design with components and other accessories
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.
Startup Company Leaders
For more information about this event please visit
https://compliancetrainings.com/SiteEngine/Product...