2 research outputs found

    Suklastotų medicinos gaminių aptikimas ir tyrimas Slovėnijoje

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    This article provides insights into the detection, investigation and prosecution of counterfeit medical products in Slovenia and abroad. The article summarizes the reports of Interpol and the European Union’s activities in this area. It also uses the opinions and insights of experts in the field provided through interviews. While the scope of the problem surrounding counterfeit medical products has been increasing globally, the issue is not alarming in Slovenia. Counterfeit medical products (CFMP) were never found to enter the legal supply chain in Slovenia. In general, the incidence of counterfeit medical products in the scope of detection, investigation and prosecution is extremely low. The reasons for this may be in the ongoing debates about the definition of CFMPs and the continuing lack of public awareness about counterfeit medical products. If the public does not understand or even know about counterfeit medical products, they will fail to report potential encounters with them, thus making their detection even more difficult. The research study presented in this paper has (partly) confirmed that a sound and socially-oriented healthcare system in which the required medicines are widely available represents a deterrent against counterfeit medical products. Therefore, the legislative framework supporting such a system is most important.Šiame straipsnyje pateikiamos įžvalgos apie suklastotų medicinos gaminių aptikimą, tyrimą ir baudžiamąjį persekiojimą už juos Slovėnijoje ir kitose valstybėse. Straipsnyje apibendrinamos Interpolo ir Europos Sąjungos veiklos šioje srityje ataskaitos, taip pat naudojamos šios srities ekspertų nuomonės ir įžvalgos, pateiktos šio straipsnio autorių atliktų interviu metu. Nors su suklastotais medicinos gaminiais susijusios problemos mastas visame pasaulyje didėja, Slovėnijoje ši problema nesulaukio didelio dėmesio. Nebuvo rasta suklastotų medicinos gaminių, kurie patektų į legalaus tiekimo grandinę. Apskritai suklastotų medicinos gaminių aptikimo, tyrimo ir baudžiamojo persekiojimo apimtys yra labai mažos. To priežastys gali būti susijusios su vykstančiomis diskusijose dėl suklastotų medicinos gaminių apibrėžimo ir nuolatinio visuomenės informuotumo apie juos trūkumu. Jei visuomenė nesupranta ar net nežino apie suklastotus medicinos gaminius, ji nepraneš apie galimus susidūrimus su jais, todėl juos aptikti bus dar sunkiau. Šiame straipsnyje pateiktas tyrimas (iš dalies) patvirtino, kad patikima ir socialiai orientuota sveikatos priežiūros sistema, kurioje reikalingi vaistai yra plačiai prieinami, galėtų būti veiksminga atgrasymo priemonė suklastotų medicinos gaminių prekybai. Todėl svarbu vystyti tokią sistemą palaikančią teisinę bazę

    Detection and Investigation of Counterfeit Medical Products in Slovenia*

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    This article provides insights into the detection, investigation and prosecution of counterfeit medical products in Slovenia and abroad. The article summarizes the reports of Interpol and the European Union’s activities in this area. It also uses the opinions and insights of experts in the field provided through interviews. While the scope of the problem surrounding counterfeit medical products has been increasing globally, the issue is not alarming in Slovenia. Counterfeit medical products (CFMP) were never found to enter the legal supply chain in Slovenia. In general, the incidence of counterfeit medical products in the scope of detection, investigation and prosecution is extremely low. The reasons for this may be in the ongoing debates about the definition of CFMPs and the continuing lack of public awareness about counterfeit medical products. If the public does not understand or even know about counterfeit medical products, they will fail to report potential encounters with them, thus making their detection even more difficult. The research study presented in this paper has (partly) confirmed that a sound and socially-oriented healthcare system in which the required medicines are widely available represents a deterrent against counterfeit medical products. Therefore, the legislative framework supporting such a system is most important
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