Medfiles is a dynamic European CRO that supports its clients on the path of commercialization with an array of services related to human and veterinary medicines, food & feed and food ingredients, medical devices, invitro diagnostical tests and cosmetics. We aim to strengthen our position as the leading CRO in Europe – by being a one-stop service provider.

We offer a complete range of product development process, starting with pharmaceutical development with quality control laboratory analyses (chemical and microbiological), implementing clinical trials and dealing with regulatory affairs (e.g. marketing authorization, pharmacovigilance). Our client base is varied but includes both small and large Pharma, Biotech, Medical device, Veterinary, Public health authorities, CMO & CROs.  

We serve companies globally. Our core competence is in the European market but we are also continuously strengthening our expertise in other market areas in order to increase our international presence as a premium quality service provider and CRO.  

To work with Medfiles, means you work with a company that has over 35 years of experience and a long list of international clients & references to prove its worth. With a team of about 180 experts, Medfiles solidly supports its clients through an offering of services that meets the ever-evolving requirements of the healthcare industry. Our contribution to bringing better and safer healthcare solutions for patients and consumers is the priority and the driving force behind our decision-making. We are securing healthier tomorrow together with our clients.

Clinical Trials

Medical Devices

Pharmaceutical

Medfiles

The Tampere office specializes in regulatory affairs, translation, and project management for food, medical devices, and pharmaceuticals.

Tampere

Medfiles' headquarters in Kuopio, Finland

The Ziepniekkalns office focuses on regulatory compliance and medical oversight within the healthcare sector.

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