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Selected aspects of the state health policy during the first wave of the Sars-Cov-2 pandemic

Płonka-Syroka Bożena, Stych Marek, Kmak Małgorzata, Pawlica Beata

Zeszyty Naukowe. Organizacja i Zarządzanie / Politechnika Śląska

2023

z. 168

365--374

Purpose: The authors analyze the decisions made from March to September 2020 which affected the functioning of Polish health care facilities. According to the authors, that period determined and significantly influenced the decisions taken by state authorities during the subsequent waves of the SARS-CoV-2 pandemic. Design/methodology/approach: The analysis of the issue presented in the paper will be a descriptive one. The research exploration will be carried out using the desk research method. Findings: Analyses of secondary and compilation documents showed that the authorities of the Republic of Poland were not prepared to manage the state in unprecedented conditions caused by the first wave of the pandemic, and the decisions taken at that time by public administration bodies were chaotic, not always well thought out and often influenced by public opinion. Originality/value (mandatory) The article can be considered original due to the fact that it combines an analysis of Polish legal acts issued during the first wave of the COVID-19 epidemic with, above all, an analysis of their social effects. The analyses showed that Polish authorities were not prepared for the pandemic crisis. The article is addressed to state administration employees as well as employees and students of universities with majors in national defense, public safety, medicine, medical rescue and public health. It may become a basis for developing legal acts of a preventive nature, which can be immediately applied in the event of another epidemic.

The falsified medicines directive and legal guarantees to ensure authenticity of medicines. The impact of drug serialization on medicine safety in the EU

Stych Marek

Zeszyty Naukowe. Organizacja i Zarządzanie / Politechnika Śląska

2019

z. 139

551--558

The aim of this study is to present the impact of the new legal solutions introduced in the so-called Falsified Medicines Directive on medicine safety in the EU. For the purposes of this study, it was necessary to analyze and interpret the provisions of the said Directive and the Delegated Regulation. The guarantees of medicine authenticity, such as a code to be scanned and placed on the medicine packaging (serialization) have been discussed in the paper. These activities are aimed at reducing the market of counterfeit medicines across the EU. The research tool used in the study was the dogmatic and legal method, which made it possible to conclude, that the provisions of the Falsified Medicines Directive increase the guarantee of drug safety. Considering the fact that these regulations are apolitical, one can assume that they will be implemented in other legal systems.