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A New Look at Informed Consent for Cancer Clinical Trials

Informed consent is fundamental to the conduct of clinical trials. Prospective participants need to be adequately informed and given the opportunity to ask questions and consult with relatives or friends without feeling pressured or rushed.

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書誌詳細
主要な著者: Baer, Allison R., Good, Marge, Schapira, Lidia
フォーマット: Artigo
言語:Inglês
出版事項: American Society of Clinical Oncology 2011
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3140452/
https://ncbi.nlm.nih.gov/pubmed/22043194
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1200/JOP.2011.000347
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