MEDFILES’ GMP-licence was extended with certification of finished products for the market. Medfiles offers you a “one-stop-shop” service package with pharmaceutical development, pharmaceutical documentation services, regulatory affairs, analytical services and Qualified Person (QP) services. For further details please contact R&D and Laboratory Services Director Mirja Savolainen: mirja.savolainen@medfiles.eu. We are looking forward to hearing from you!