THE IMPORTANCE OF GMP AND ISO STANDARDS IN THE PHARMACEUTICAL INDUSTRY
DOI:
https://doi.org/10.5281/zenodo.17510004Keywords:
GMP, ISO, pharmaceutical industry, quality system, standardization, safety, quality assurance.Abstract
This article analyzes the significance of quality management systems — GMP (Good Manufacturing Practice) and ISO (International Organization for Standardization) — in the pharmaceutical industry. The theoretical foundations and practical implications of these standards are discussed in relation to their impact on the quality, safety, and stability of pharmaceutical products. The paper also explores the integration of GMP and ISO principles within the context of Uzbekistan’s pharmaceutical industry and its prospects for global competitiveness.
References
World Health Organization (WHO). Good Manufacturing Practices: Main Principles for Pharmaceutical Products. Geneva, 2021.
International Organization for Standardization (ISO). ISO 9001: Quality Management Systems – Requirements, 2015
Ministry of Health of the Republic of Uzbekistan. Concept for the Development of the Pharmaceutical Industry, 2023.
Sharma, P., et al. Integration of GMP and ISO Systems in Modern Pharmaceutical Industry. Journal of Pharmaceutical Quality, 2022.
Alimov, B., et al. Quality Systems in Pharmaceutical Technology and Their Control. Tashkent, 2021.
