Finnish Medicines Agency Fimea maintains a list of all granted and cancelled marketing authorisations, parallel imported medicinal products and registrations. The list is published once a month by the 15th of each month, and it contains information for the previous month.
The list does not include marketing authorisation issues covered by the centralised procedure; requests for information regarding these should be submitted to the European Medicines Agency EMA.
Requests for other Fimea documents should be submitted to:
Finnish Medicines Agency Fimea
P.O. Box 55 (Mannerheimintie 103b)
FI-00034 FIMEA, FINLAND