Principles of QMS documents system for medical drugs manufacturers
Автор: Dyakonova E.V., Ruban T.I.
Журнал: Сибирский журнал клинической и экспериментальной медицины @cardiotomsk
Рубрика: Организация производства медицинских препаратов
Статья в выпуске: 2-2 т.26, 2011 года.
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Today there exists no universal approach to the construction of the documentation system as one of the bases for the organization of the medical drugs manufacture in compliance with the GMP requirements, which has made it necessary. As a result, it is necessary to develop new methods of making and operating QMS documents with regard to medical drugs manufacturers.
Quality management system (qms), internal controlled documents, standard operational procedure (sop)
Короткий адрес: https://sciup.org/14919468
IDR: 14919468
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