Legal regulation and standardization of drugs: analysis of key standards

Yoqubova, Umidakhon, Ёкубова, Умидахон, Yoqubova, Umidaxon

Жамият ва инновациялар / Общество и инновации / Society and innovations · 2025-yil

Annotatsiya

The modern development of the pharmaceutical industry is impossible without an effective and scientifically based system for regulating the quality, safety, and effectiveness of medicines. In the context of globalization and Uzbekistan's integration into the international pharmaceutical space, proper practice standards covering all stages of the drug lifecycle are gaining particular importance. This article is dedicated to a comprehensive analysis of key standards such as Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), Good Storage Practice (GSP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Pharmacy Practice (GPP), which have been legally enshrined in the legislation of the Republic of Uzbekistan. The article reveals the essence, structure, and legal nature of each standard, as well as their significance for state regulation, consumer protection, and increasing the competitiveness of pharmaceutical products. Special attention is paid to the analysis of the regulatory framework, the dynamics of implementation of standards, and their role in strengthening confidence in the national healthcare system. The work aims to form a holistic understanding of the legal and practical aspects of standardization in the pharmaceutical field and can be useful for both researchers and industry practitioners.

Maqola ma’lumotlari
MualliflarYoqubova, Umidakhon, Ёкубова, Умидахон, Yoqubova, Umidaxon
JurnalЖамият ва инновациялар / Общество и инновации / Society and innovations
Nashr sanasi2025-04-25
Jild6
Son4/S
Betlar601-609
TilRus
DOI10.47689/2181-1415-vol6-iss4/s-pp601-609

Kalit so‘zlar

Лекарственные средства, стандартизация, надлежащая практика, GMP, GDP, GSP, GCP, GLP, GPP, фармацевтическое регулирование, система качества, Узбекистан, законодательство, сертификация, Medicines, standardization, Good Practice, GMP, GDP, GSP, GCP, GLP, GPP, pharmaceutical regulation, quality system, Uzbekistan, legislation, certification, Dori vositalari, standartlashtirish, to‘g‘ri amaliyot, GMP, GDP, GSP, GCP, GLP, GPP, farmatsevtik tartibga solish, sifat tizimi, O‘zbekiston, qonunchilik, sertifikatlashtirish

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