We at Medfiles, in collaboration with our partner Link Medical Research, can help you and provide you with local pharmacovigilance services in all Nordic and Baltic countries. Our pharmacovigilance team is happy to help you with for example:
· receipt of adverse event reports
· follow-up
· support in reconciliation processes
· translation of adverse event reports and other pharmacovigilance documentation
· acting as a contact person for local authorities
· monitoring of local literature
For more information, visit our web page or contact
Satu Kujala
Clinical Research Director
satu.kujala@medfiles.eu or expert@medfiles.eu
Tel. +358 50 577 9003
