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.
In response to the Covid-19 emergency, the European Commission released a proposal to amend certain provisions of the Medical Device Regulation (EU) 2017/745.
Today’s live read-out by the European Commission spokesperson Stefan De Keersmaecker announced a proposal to delay the application of the new MDR.
As the COVID-19 emergency impacts all healthcare sectors, Meditrial provides rapid tools to help industry and researchers rescue their clinical trials.
We set up a Meditrial FREE HELPLINE, a tool to facilitate communication with our teams and address any particular questions or new requirements.
The New York City office is a brand new space to bring together people who share a dedication to innovation. Come visit the Training Center.
Complex new rules will impact the daily work of economic operators, healthcare professionals and health institutions. Learn how to get ready.
The workshop “MDR MASTER CLASS” blends Academy and Industry to offer the most modern education for Medtech and Clinical Professionals
A practical course from experts who manage top medtech trials in Germany. CME 8 Points
Best way to manage is still unclear, but routine anticoagulation and close follow-up seem warranted.
