Risk Management Plan Template (Medical Device and ISO 14971)

49.00 (ex. GST/VAT)

This template will provide you with a framework to complete your risk management plan according to ISO 14971:2019 and MDR. The template includes topics as required by clause 4.4 of ISO 14971:2019 and references software risk management according to IEC 62304:2006.

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Why it is useful

A risk management plan is required because an organized approach is essential for effective risk management, the plan provides the roadmap for risk management, encourages objectivity and helps prevent essential elements being forgotten.

How to use it

1. If you are developing a brand-new product, establish as much as possible of this plan in the planning phase of your project.
2. If you are making a revision of an old product, or adding a product to a range that this plan applies to, the plan might only have to be updated slightly.
3. Note that the plan shall be maintained, that is, it should reflect what you are doing and the other way around.


If you have questions about the content of the template, you may ask questions in the support forum up to 10 days after your purchase. The support forum is accessible on this link when you are logged in to you account. You you can see other previously asked questions as well as ask any questions you may have.

Need risk management training and a course certificate?

Take a look at our online course: Introduction to Risk Management for Medical Devices and ISO 14971. Learn about the overall process of risk management, the tools and techniques used and how to develop a safe medical device according to regulatory requirements. Created by industry experts. Certification on successful completion of course.


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