- A quick and easy introduction to working with the EU MDR
- Understand key requirements and build a foundation for compliance
- Understand your obligations as a medical device manufacturer
- See how QMS, PMS, PMCF, Risk Management & Clinical Evaluation integrate to form a mature system
- Begin planning timelines and resource requirements necessary to gain approval for your devices
EnableCE Build MDReady Starter Guide
Our free step-by-step guide is the start of your journey to EU MDR compliance
Guide overview
- 23-page PDF document
- A quick and easy introduction to working with the EU MDR
- Understand key requirements and build a foundation for compliance
- Understand your obligations as a medical device manufacturer
- See how QMS, PMS, PMCF, Risk Management & Clinical Evaluation integrate to form a mature system
- Begin planning timelines and resource requirements necessary to gain approval for your devices
In more detail
A simple, comprehensive and free guide to working with the EU MDR.
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This guide is suitable for complete beginners but will be of value to those with a bit more experience in medical device regulation.
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An easy-to-use PDF document to work through at your own pace.
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Begin your EU MDR compliance journey with a degree of confidence and enable you to make the most of our services and EnableCE.
Free download
You can use your free download immediately after download.
MDReady Starter Guide
- 23-page PDF document
Our free step-by-step guide is the start of your journey to EU MDR compliance
FREE
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