Regulatory affairs

Our regulatory services not only cover the Scandinavian and the Baltic countries, but extend to Western, Central and Eastern European countries through our regulatory network.

We offer you a complete, accurate, up-to-date service for the entire life cycle of your product. Services are always tailored to meet your precise needs. We are committed to ensure that our efforts will benefit your product development.

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.

We are pleased to help you when your regulatory needs concern:

• human medicinal products
• veterinary medicinal products
• herbal medicines
• medical devices
• food supplements

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.

Contact persons:

Regulatory Affairs / Baltic countries

Regulatory Affairs Manager
Heidi Tikerpe
Tel.     +372 7305 426
Mobile +372 5291 111
E-mail: heidi.tikerpe(at)medfiles.eu
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