Legal Protection of Subjects' Informed Consent in Clinical Drug Trials / 中国药房
China Pharmacy
;
(12)2007.
Artigo
em Chinês
| WPRIM
| ID: wpr-531196
ABSTRACT
OBJECTIVE:
To provide the reference for the improvement of GCP(good clinical practice)regulations and protection of subject's human rights.METHODS:
The status quo of the protection of subject's right of informed consent and the elements for the right of informed consent and the existing problems in its practice in China were analyzed.RESULTS &CONCLUSIONS:
China should further promote the legislation of clinical trials,reinforce the legal education of researchers,and emphasize the supervision on the illegal tort act.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Idioma:
Chinês
Revista:
China Pharmacy
Ano de publicação:
2007
Tipo de documento:
Artigo
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