Rules for medicinal products

1. Rulebook on the contents and method of labelling the outer and immediate packaging of a medicine, additional labelling, and contents of the package leaflet (“Official Gazette of RS”, No. 41/2011)

2. Rulebook on the Contents of the Application, and/or Documentation on the Approval of Clinical Trials for Medicines and Medical Devices, as well as the Method of Implementation for Clinical Trials of Medicines and Medical Devices (“Official Gazette of RS”, No. 64/2011)

3. Rulebook on the method of reporting, collecting and monitoring adverse reactions to medicines (“Official Gazette of RS”, No. 64/2011)