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Updated: May 28, 2026

Working with Human Tissues for Translational Cancer Research
Published on: November 26, 2015
A new look at informed consent for cancer clinical trials
Allison R Baer1, Marge Good, Lidia Schapira
1American Society of Clinical Oncology, Alexandria, VA; Community Oncology and Prevention Trials Research Group, Division of Cancer Prevention, National Cancer Institute, Bethesda, MD; Harvard Medical School; Masschusetts General Hospital, Boston, MA.
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.
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