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- W103630273 abstract "Informed consent is obtained from a possible participant in a clinical trial primarily to protect the rights, safety, well being, and interests of those participating in the trial. Written consent has been developed to avoid coercive or deceptive recruitment and the use of unethical enrolling practices." @default.
- W103630273 created "2016-06-24" @default.
- W103630273 creator A5043050851 @default.
- W103630273 date "2009-01-01" @default.
- W103630273 modified "2023-09-26" @default.
- W103630273 title "Informed consent forms" @default.
- W103630273 doi "https://doi.org/10.1007/978-3-7643-8362-6_10" @default.
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