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.
CITATION STYLE
Targeted Regulatory Writing Techniques: Clinical Documents for Drugs and Biologics. (2009). Targeted Regulatory Writing Techniques: Clinical Documents for Drugs and Biologics. Birkhäuser Basel. https://doi.org/10.1007/978-3-7643-8362-6
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