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Abreast of global regulations and industry standards.

Minimally invasive heart valves
Dr, Monica Tocchi, the only Italian expert in the ISO 14155 technical committee, appointed in technical committee for the development of standard ISO 5840 "Cardiovascular Implants - Cardiac Valve Prostheses. Part 3 - Hear Valve Substitutes implanted by minimally invasive techniques."

  • Clinical fast track to market.

    Clinical fast track to market.

    published Saturday, May 7, 2011

    Clinical results are the central element for any medical therapy. The right approach for presenting the data will speed up market approval and support rapid adoption of new technologies.

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More trial. Less error. »

Bringing cutting edge therapies to market, structuring successful clinical trials, navigating regulatory issues-all can be complicated, even frustrating challenges.

At Meditrial, we believe our role is to minimize complexity, eliminate wasted time and resources. With the right team and technological tools, we'll meet your needs effectively, and on time.


GCP for device trials. » 

Regulations for conducting medical device clinical trials around the world have varied widely. Data may be questionable given different requirements.

Experts from the United States, Europe, and Japan have agreed on a new standard - ISO 14155 - that helps to level the field among countries and enhances trial acceptance and quality.