MOTIVATION AND PARTICIPATION EXPERIENCE OF HEALTHY VOLUNTEERS IN THE CLINICAL TRIALS OF BIOEQUIVALENCE IN RUSSIA

The definition of safety, tolerability and efficacy of drugs is largely related with the results of clinical trials (CTs). Currently, phase I studies, pharmacokinetics and bioequivalence, conducted with the participation of healthy volunteers, are one of the main ways to registering drugs in our cou...

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Detalhes bibliográficos
Main Authors: I. V. Mareev, I. A. Samykina, M. Y. Kolokoltsova, I. D. Pimenov, M. S. Tomofeev, E. S. Kulikov, I. A. Deev, E. V. Borodulina, O. S. Kobyakova, V. V. Udut
Formato: Artigo
Idioma:Russo
Publicado em: LLC Center of Pharmaceutical Analytics (LLC «CPHA») 2019-01-01
Colecção:Разработка и регистрация лекарственных средств
Assuntos:
clinical trials
bioequivalence
perception
motivation
Acesso em linha:https://www.pharmjournal.ru/jour/article/view/565
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