Changes to delivery of documents concerning clinical trials
From 1 January 2018 all documents concerning changes to clinical trial research plans must be delivered to Fimea both in paper and electronic format (on a CD).
This has already applied to documents concerning new clinical trial notices from 1 January 2017.
For the time being paper versions are needed for archiving purposes.
- Suvi Mantere, Clinical Trials Coordinator, tel. +358 29 522 3390
- Eija Mikkonen, Clinical Trials Coordinator, tel. +358 29 522 3393
- The e-mail addresses have the form email@example.com.