Clinical trials

The main focus of our clinical research is in the Nordic countries (Finland, Sweden, Norway and Denmark) and the Baltic countries (Estonia, Lithuania and Latvia). More than 100 million people live in this region, which makes it possible to conduct very large studies. We cooperate with our CRO partners in numerous European countries, as well as with CROs operating in the rest of the world (e.g. China).

We offer you comprehensive services for Phase I–IV studies, from study initiation to final reporting, including protocol preparation, project management, monitoring, statistical evaluation and data management. We also provide outsourcing services: our personnel can work either at Medfiles premises or at your premises.

We can also help you with register studies, health economics in clinical trials, medical device trials, and consultation and training.

We have experienced, enthusiastic and committed personnel who take pride in what they do. Our personnel undergo continuous training to ensure that you receive services of the highest quality.

Flexibility, Freshness and Fairness based on the experience and competence of our team ensure the quality of all our work. “One-stop-shop“ service package is designed to encompass all your needs concerning clinical trials.

Experience

Clinical trials by phase since 2000:

Clinical trials by therapeutic area since 2000:
For more information, please click the therapeutic area below you are interested in:

Contact persons

Clinical Research Director
Anja Taube-Siikavirta
Tel. +358 20 7446 878
Mobile +358 50 359 0655
E-mail: anja.taube-siikavirta(at)medfiles.fi

Clinical Trials / Baltic countries

Clinical Research Manager
Lemme Urmet
Tel. +372 7305 403 / +372 7305 419
Mobile +372 5279 229
E-mail: lemme.urmet(at)medfiles.eu

www.medfiles.eu

Quality assurance (QA)