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- Mastering the MDR — This White Paper summarises the MDR and makes its contents easy to digest. It is intended to highlight those areas in the text that are most relevant to medical device manufacturers.
- PMS in the MDR — The MDR places a higher burden on manufacturers in many areas including Post-Market Surveillance system design, implementation and reporting. This White Paper offers guidance on the requirements for PMS in the MDR.
- Software as a medical device — Understand when and why the MDR applies to medical software, a rapidly growing sector of the medical device market. Learn whether or not the MDR will apply to your software product and how to work with the new legislation.
- MDR Requirements Matcher — This tool will instantly navigate Annex I MDR, quickly showing you which GSPRs apply to your products without the need to manually search.