Meditrial is a leading Clinical Research Organization (CRO) focused on the needs of the MedTech industry. We are proud to serve the most innovative companies in the world. Our staff is recognized by customers and investigators as more expert, trustworthy and responsive – our people get the job done right.
for Rapid CE mark
Empowering Upgrades of Clinical Evaluation
- With the change of European regulation, medical device companies must produce new clinical reports to achieve or maintain their CE mark
- Meditrial created an easy method to upgrade any clinical evaluation to the new guidelines, MEDDEV 2.7.1 Rev 4
- Over 100 reports were produced by Meditrial for a range of technologies spanning from implantable cardiac devices, to ablation technologies or non-invasive diagnostics and many more.
- All clinical evaluations produced by Meditrial experts were audited and approved by multiple notified bodies, including BSI, DEKRA, TUV PS, LNE-GMED, and others.
"Our CER was reviewed and passed with flying colors. Please know how much we appreciated your support" - David H. , Quality Director, Profusa Inc., San Francisco