According to the provision of Article 4 of the Supply of Blood Act (Official Gazette of the Republic of Slovenia [Uradni list RS], No. 104/2006, below: ZPKrv-1) JAZMP supervises the implementation of provisions from this Act and the regulations and general legal acts that were issued on the basis of the Act. In accordance with Article 7 of ZPKrv-1, JAZMP performs periodic inspections in blood transfusion institutions or transfusion centres and sets suitable control measures to deal with any serious adverse events or serious adverse reaction or suspicion of the latter. According to Article 166 of the Medicinal Products Act (Official Gazette of the Republic of Slovenia [Uradni list RS], No. 17/2014, below: ZZdr-2), inspections are performed by pharmaceutical inspectors with authorisations in accordance with paragraph two of Article 166 of ZZdr-2 as determined in the Inspection Act (Official Gazette of the Republic of Slovenia [Uradni list RS], No. 43/2007 – official consolidated text, and 40/2014, below: ZIN-B).
In case of an identified infringement of provisions of ZPKrv-1 or a suspicion of violation, JAZMP acts in accordance with the provisions of the of the Minor Offences Act.