MDR Risk Management training course - Build, document & maintain an ISO 14971:2019-compliant system

Build an entire Risk Management system for all your medical devices. This training course is designed for people who want to produce complete Risk Management systems in-house. It is suitable for QA/RA professionals with existing knowledge of the EU MDR and company founders during early stage product development. The course will allow you to confidently build a complete Risk Management system from start to finish for your entire portfolio of medical devices.
Our training courses are broken up into chapters and short, streamable videos which save your progress automatically. Downloadable documents are included to support your learning. All our training courses are on-demand and can be completed to your schedule in the comfort of your own workspace. You won't have travel or accommodation costs, or any other expenses usually incurred whilst away from your workspace.
- Understand the structure, key requirements & terminology of ISO 14971:2019
- Learn how to correctly apply Risk Management principles to the entire life cycle of a device
- Gain complete understanding of each stage of the Risk Management process
- Confidently produce all essential documents and efficiently manage updates
- Learn how to integrate Risk Management with QMS, PMS & broader regulatory activities
- Identify opportunities for product improvement & competitive advantage
For more information please visit:
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