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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Bibliographic Details
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
Format: Article
Language:Russian
Published: LLC Center of Pharmaceutical Analytics (LLC «CPHA») 2019-01-01
Series:Разработка и регистрация лекарственных средств
Subjects:
Online Access:https://www.pharmjournal.ru/jour/article/view/565