Protection of Informed Consent Rights for Subjects in Drug Clinical Trials / 中国医学伦理学
Chinese Medical Ethics
; (6): 840-846, 2023.
Article
en Zh
| WPRIM
| ID: wpr-1005638
Biblioteca responsable:
WPRO
ABSTRACT
The right to informed consent is the basic right of subjects in drug clinical trials. International treaties and domestic laws have successively formed a basic right protection framework, while there are still some problems such as imperfect legal norms and incomplete practical operations. To meet future challenges, it is necessary to further improve legislation, standardize notification procedures, improve notification content, expand dynamic notification methods, and strengthen ethical review, so as to build a standardized and modern system for protecting the right to informed consent of subjects.
Texto completo:
1
Base de datos:
WPRIM
Idioma:
Zh
Revista:
Chinese Medical Ethics
Año:
2023
Tipo del documento:
Article