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