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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
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