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A new look at informed consent for cancer clinical trials. Journal of oncology practice Baer, A. R., Good, M., Schapira, L. 2011; 7 (4): 267-70
Abstract
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.
View details for DOI 10.1200/JOP.2011.000347
View details for PubMedID 22043194
View details for PubMedCentralID PMC3140452