FARMASEVTIKADA GMP (GOOD MANUFACTURING PRACTICE) STANDARTLARINING AHAMIYATI
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Аннотация:
Mazkur maqolada farmatsevtik sanoatda GMP (Yaxshi ishlab chiqarish amaliyoti) tamoyillarining ahamiyati va ularning sifatli, xavfsiz dori vositalarini ishlab chiqarishdagi o‘rni yoritib berilgan. GMP tamoyillarining har bir bosqichi: standartlashtirilgan protseduralar, xodimlar malakasi, ishlab chiqarish hududi, xomashyo sifati, mahsulotni hujjatlashtirish, test va nazorat jarayonlari, mahsulotni kuzatish va qaytarib olish tizimi hamda ichki auditlar haqida batafsil ma’lumot beriladi. Maqolada xalqaro tashkilotlarning ma’lumotlari, O‘zbekistondagi holat bo‘yicha statistikalar va ilmiy tadqiqotlar asosida tahlil qilinadi. Kelajakda GMP talablarining yanada keng joriy etilishi farmatsevtik mahsulotlar sifatining oshishiga xizmat qilishi ta’kidlanadi. Shuningdek, muallifning ushbu sohaga oid shaxsiy kuzatuv va umidlari ham bayon etilgan.
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Библиографические ссылки:
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