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Medical Device CE marking
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Medical Device Manufacturers seeking CE marking or already CE marked, click on each card to discover how Certeafiles simplifies the creation and management of MDR (EU) 2017/745 technical documentation.
50+
document templates covering the entire MDR (EU) 2017/745 framework
6+1
6 steps to achieve CErtification, 1 continuous process to maintain it
50%
time saved on creating and managing your technical documentation
Personalized Support
At Certeafiles, we believe that technology becomes truly powerful when it’s backed by human expertise. Our specialists in medical device regulation and quality put their know-how at your service to design a strategy tailored to your needs. From training to auditing, through consulting, each service is designed to strengthen your skills and secure your compliance processes — letting digital tools do the work while our partners and experts step in where human insight adds the greatest value.
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