Consent Requirements for Testing Health Policies: An Intercontinental Comparison of Expert Opinions

Individual informed consent is a central requirement for clinical research on human subjects, yet whether and how consent requirements should apply to health policy experiments (HPEs) remains unclear. HPEs test and evaluate public health policies prior to implementation. We interviewed 58 health exp...

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Detalles Bibliográficos
Autores principales: Berner-Rodoreda, Astrid, McMahon, Shannon, Eyal, Nir, Hossain, Puspita, Rabbani, Atonu, Barua, Mrittika, Sarker, Malabika, Metta, Emmy, Mmbaga, Elia, Leshabari, Melkizedeck, Wikler, Daniel, Bärnighausen, Till
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Empirical Studies of Issues in Informed Consent
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136368/
https://www.ncbi.nlm.nih.gov/pubmed/35617114
http://dx.doi.org/10.1177/15562646221076764

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136368/
https://www.ncbi.nlm.nih.gov/pubmed/35617114
http://dx.doi.org/10.1177/15562646221076764

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