[The management in clinical trials of pharmacological agents]

Autor:	L V, Kurmanova
Rok vydání:	1995
Předmět:	Quality Control Clinical Trials as Topic Pharmaceutical Preparations Research Humans
Zdroj:	Problemy sotsial'noi gigieny i istoriia meditsiny. (5)
Popis:	The author analyzes the experience gained by foreign countries in the creation of a new management system in all spheres of public health, including clinical trials and use of drugs. A term "High-Quality Clinical Practice" is used in the European Community, reflecting the standard or the norm of clinical studies and designed as a complex of regulations for the organization and implementation of clinical studies. High-Quality Clinical Practice implies all reasonable measures providing the accuracy of experimental data and guarantees the rights of the participants in the trials. Studies carried out in conformity with the requirements of High-Quality Clinical Practice bring about reliable results and permit the pharmaceutical companies and public health organs use these data.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::d14546dd95c16006b58626af85fec386 https://pubmed.ncbi.nlm.nih.gov/9273153 Zobrazit plný text záznamu