DORI VOSITALARINI SAQLASH VA TASHISHDA SIFATNI TA’MINLASH
Keywords:
dori vositalari, saqlash, tashish, sifatni ta’minlash, GDP, GMP, logistikaAbstract
Ushbu maqolada dori vositalarini saqlash va tashish jarayonlarida ularning sifati,
xavfsizligi va samaradorligini ta’minlash masalalari yoritilgan. Saqlash sharoitlari
(harorat, namlik, yorug‘lik), tashish vaqtida yuzaga keladigan xavf omillari hamda
xalqaro GMP va GDP talablariga rioya qilishning ahamiyati tahlil qilingan. Dori
vositalarining sifatini saqlab qolishda logistika tizimi va monitoring usullarining o‘rni
ko‘rsatib berilgan.
References
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World
Health
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https://www.who.int/publications/i/item/WHO-TRS-957
2.
World Health Organization (WHO).
Good Manufacturing Practices (GMP) for pharmaceutical products.
https://www.who.int/teams/health-product-policy-and-standards/standards-and
specifications/gmp
3.
European Commission.
Guidelines on Good Distribution Practice of medicinal products for human
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https://health.ec.europa.eu/medicinal-products/eudralex/eudralex-volume-4_en
4.
United States Pharmacopeia (USP).
USP <1079> Good Storage and Shipping Practices.
https://www.usp.org/compounding/general-chapter-1079
5.
ICH (International Council for Harmonisation).
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https://www.ich.org/page/quality-guidelines
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Aulton, M. E., Taylor, K.
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https://www.elsevier.com/books/aultons-pharmaceutics
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Yuldashev A., Karimov R.
Farmatsevtik logistika va dori vositalarini saqlash asoslari.
Toshkent, 2020.
(mahalliy darslik, bosma manba)
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WHO & UNICEF.
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