Quality Standards of Preclinical Pharmacological Studies

The quality and effectiveness of preclinical trials of medicines depend on compliance with the Good Laboratory Practice (GLP) principles. At the same time, the data of the World Health Organisation (WHO) and the analysis of the regulatory framework suggest that the reliability and reproducibility of...

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Bibliografski detalji

Glavni autori:	G. N. Engalycheva, R. D. Syubaev, D. V. Goryachev
Format:	Artigo
Jezik:	Russo
Izdano:	Federal State Budgetary Institution ‘Scientific Centre for Expert Evaluation of Medicinal Products’ of the Ministry of Health of the Russian Federation (FSBI ‘SCEEMP’) 2019-12-01
Serija:	Регуляторные исследования и экспертиза лекарственных средств
Teme:	medicines basic biomedical research preclinical research primary pharmacodynamics secondary pharmacodynamics safety pharmacology quality practice in preclinical research
Online pristup:	https://www.vedomostincesmp.ru/jour/article/view/225
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