Placing a medicine on the market

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

Import and export of medicines

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

Controlled substances

Institute is responsible for issuance of authorisations for drugs and precursors

Clinical trials

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

Consumption of medicines

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

Maximum prices of medicines

Institute sets maximum prices for medicines for human use

Medicines quality defects

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

Register of human medicines

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