Comparison of requirements for storage of drugs that regulated good storage practice and license terms

dc.contributor.authorMolodozhonova, O.
dc.contributor.authorSuhovoy, H.
dc.contributor.authorBushueva, I.
dc.contributor.authorМолодожонова, Ольга Олександрівна
dc.contributor.authorСуховой, Григорій Пилипович
dc.contributor.authorБушуєва, Інна Володимирівна
dc.date.accessioned2020-05-07T07:01:45Z
dc.date.available2020-05-07T07:01:45Z
dc.date.issued2015
dc.description.abstractOne of the urgent issues of modern pharmaceutical institutions is the creation and implementation of quality assurance, in the context of which and subject to the applicable legislation, more specific are the requirements for quality control of medicines and the conditions of their storage and research of the industry relevant and timely. Thus, as a result of the study we made a comparative analysis between the licensing conditions and standards of good practice we have offered detail requirements for the storage of drugs and we have offered requirements for the authorized person.uk_UK
dc.identifier.citationMolodozhonova O. Comparison of requirements for storage of drugs that regulated good storage practice and license terms / O. Molodozhonova, H. Suhovoy, I. Bushueva // lntellectual Aгchive. – 2015. – Vol. 4, №6. – P. 39-43.uk_UK
dc.identifier.urihttps://zsmu.rosbai.com/handle/123456789/10946
dc.language.isoenuk_UK
dc.publisherShiny World Corporation, Toronto, Canadauk_UK
dc.subjectgood storage practiceuk_UK
dc.subjectlicensing conditionsuk_UK
dc.subjectmanagement of pharmaceutical establishmentsuk_UK
dc.subjectmedicinesuk_UK
dc.subjectEuropean Unionuk_UK
dc.titleComparison of requirements for storage of drugs that regulated good storage practice and license termsuk_UK
dc.typeArticleuk_UK

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