С 30 июля 2011 вступило в силу Постановление СТ-Н МОЗУ 42-4.0:2011 «Лекарственные средства. Надлежащая производственная практика »,
утвержденная приказом Минздрава Украины от 06.07.2011 № 392. Изменения внесены в раздел 4 «Документация» Части I и приложение 11 «Компьютеризированные системы» руководства в соответствии с изменениями в GMPЕС.
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The information on this page is intended for scientific, educational, and general informational purposes. Clinical approaches, availability, and regulatory status may vary by country, institution, and medical indication. For individual medical decisions, readers should consult qualified healthcare professionals and accredited medical centers.
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This article has been prepared by the NBScience editorial team within the scope of clinical research, biotechnology, and international medical information.
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