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Marketing authorisation

A medicinal product must have a valid marketing authorisation before it can be introduced on to the market and submitted for distribution.

Medicinal products also include herbal medicinal products and homeopathic anthroposophical products. Further information about the procedures for their marketing authorisation and registration can be found at Herbal Remedy.

The procedures for veterinary medicinal products are explained at Veterinary Medicines.

Information about medicinal products available on the market including dates of marketing authorisation approval is available via medicinal product search.

Further information:

  • Section for Innovative Medicines: Marja Helenius, Procedure Manager, tel. +358-9-4733 4235
  • Section for Generic Medicines: Leena Pietilä, Procedure Manager, tel. +358-9-4733 4436
  • Section for Veterinary Medicines: Heidi Mustalammi, Procedure Manager, tel. +358-9-4733 4286

E-mail addresses: firstname.lastname@nam.fi

What's new

>  11.1.2010
New regulation 1/2009 on applying for and maintaining a marketing authorisation and registration for a medicinal product

23.12.2009
Request for time slot for applications via the Decentralised Procedure (DCP) with Finland as Reference Member State (RMS) for human use

23.12.2009
Request for Finland to act as RMS in a Mutual Recognition Procedure (MRP)