Human medicines

Placing a medicine on the market

Institute for medicines and medical devices is responsible for issuance of marketing authorization for a medicine

Institute issues consent for the import of medicines that are not authorised for marketing

Institute is responsible for issuance of authorisations for drugs and precursors

Clinical trials are fundamental for the development of innovative products: medicines and medical devices

Institute has the authority to perform collecting, processing and publishing reports on consumption of medicines in Montenegro

Institute sets maximum prices for medicines for human use

On this page you may find the information on how to report a suspected quality defect of a medicine

Information on medicines that obtained marketing authorisation issued by the Institute are available on this page