By Deborah Norris Although informed consent is required by law, it is essentially an ethical imperative grounded in the principle of respect for persons. Following this respect for people, it is crucial to have a well-written and easily comprehendible document. This handbook helps to facilitate the translation of technical terms to a more generally understandable language for clinical researchers who wish to write well. 1996/69 pp/softbound (Formerly published by Pharmaceutical Information Associates) Out of Print |
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