ISO 14971 Risk Management Training in Medical Devices is required for all medical device manufacturers. Identifying, assessing and controlling risks in a product's life cycle in medical devices helps you implement a risk management framework within a continuous compliance framework. At the end of this training, you can have all the tools to manage your risks in compliance with an international standard.
Who Should Attend
• Quality Managers
• Licensing Unit Managers
• Inspectors of medical device manufacturing organizations (internal and external)
• Functional team members involved in the implementation