We can support you from initial regulatory strategy and intelligence, through the whole application process.
We have the necessary permits and licenses to support your development or manufacturing needs: EU GMP manufacturing certificate; Manufacturing license in accordance with Norwegian pharmacy law; GDP wholesaler certificate; Wholesaling permit with own warehouse (incl. narcotic and psychotropic drugs).
We advice your regulatory strategy, liaise with authorities and take care of quality agreements and supply contracts, while compiling the dossier and ensuring a smooth application process. Our services includes as well to help you bring your products to the Nordics or EU market.