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Analysis on Legal Relationship Based on a Typical Case of Medical Device Clinical Trial / 中国医学伦理学
Chinese Medical Ethics ; (6): 284-287, 2023.
Article de Zh | WPRIM | ID: wpr-1005545
Bibliothèque responsable: WPRO
ABSTRACT
Guaranteeing the rights and safety of subjects is an important responsibility of all participants in the medical devices clinical trial, including medical institutions, sponsors and researchers. The legal disputes caused by serious adverse events in the clinical trial of medical devices are characterized by complex legal relationships, great difficulty in handling, and many points of dispute. Based on a typical case of medical device clinical trials, this paper discussed the litigation subject qualification, the treatment of contract breach and tort in medical device clinical trial, analyzed the responsibility of different subjects, and provided constructive suggestions on the risk management of medical device clinical trial.
Mots clés
Texte intégral: 1 Indice: WPRIM langue: Zh Texte intégral: Chinese Medical Ethics Année: 2023 Type: Article
Texte intégral: 1 Indice: WPRIM langue: Zh Texte intégral: Chinese Medical Ethics Année: 2023 Type: Article