Farmacja Polska (Oct 2020)

Polish legal pharmaceutical market regulations since 1918

  • Małgorzata Maria Kubacka

DOI
https://doi.org/10.32383/farmpol/128608
Journal volume & issue
Vol. 76, no. 9
pp. 509 – 518

Abstract

Read online

The currently applicable legal institutions sanctioning the protection of public health in the field of pharmacy are not new - many of them have been established in Poland over the last 100 years ago. Their development was particularly visible in the interwar period, when the foundations for legal solutions applied after World War II were laid. Many legal institutions are still in use today, such as the marketing authorization, the authorization to establish a pharmacy, and quality control of the drugs on the market and many others. It can be observed evolution of legal definitions like: medicinal product, patient, marketing authorization holder. A few definition disappeared – like decayed or counterfeit medicinal product. On the base of general regulations of pharmaceutical market after years new legal acts were created like act on counteracting drug addiction or act on medical devices. There have been major changes to the criminal law. Initially, Initially, a violation of the legal provisions regarded to the production, trading or running of pharmacies and others referred to the currently applicable penal codes - until 1932 these were three post-partition codes - Russian, German and Austrian penal law. From 1932 it was adopted the Polish Penal Code, known as “Makarewicz Code”. It was not until 1951 that criminal provisions appeared in the Act of pharmacies, and since then non-code criminal law was created in the field of pharmacy. Some solutions have appeared quite recently – it can be included the requirement to conduct clinical trials before applying for marketing authorization of a medicinal product to the market or the institution of target import to save the patient's life and health. Pharmaceutical supervision in the form of the Pharmaceutical Inspection is also a result of the entry into force of the Act of 1991. Our modern pharmaceutical law is not only the result of the implementation of EU directives, but also our own Polish experience in the field of regulation of the broadly understood protection of public health, and more precisely - pharmaceutical safety.

Keywords