Issues Surrounding Biospecimen Collection and Use in Clinical Trials
Author:
Affiliation:
1. American Society of Clinical Oncology, Alexandria, VA; Research Advocacy Network, Plano, TX; Patient Advocates in Research, Danville, CA; and Duke University Medical Center, Chapel Hill, NC
Abstract
Publisher
American Society of Clinical Oncology (ASCO)
Subject
Health Policy,Oncology(nursing),Oncology
Link
http://ascopubs.org/doi/pdfdirect/10.1200/JOP.777004
Reference5 articles.
1. American Society of Clinical Oncology Statement on Minimum Standards and Exemplary Attributes of Clinical Trial Sites
2. Elements of informed consent for pharmacogenetic research; perspective of the pharmacogenetics working group
3. RETURNING GENETIC RESEARCH RESULTS TO INDIVIDUALS: POINTS-TO-CONSIDER
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1. Assessing Views on Using Surplus Human Bio Specimens for Future Research among Pharmaceutical Sponsors: A Prospective Interventional Study;Journal of Young Pharmacists;2024-08-23
2. Privacy Concerns About Personal Health Information and Fear of Unintended Use of Biospecimens Impact Donations by African American Patients;Journal of Cancer Education;2019-03-07
3. Development and validation of the biobanking attitudes and knowledge survey-Spanish (BANKS-SP);Journal of Community Genetics;2016-09-15
4. Participation in Cancer Pharmacogenomic Studies: A Study of 8456 Patients Registered to Clinical Trials in the Cancer and Leukemia Group B (Alliance);Journal of the National Cancer Institute;2015-07-09
5. Development and Validation of the Biobanking Attitudes and Knowledge Survey (BANKS);Cancer Epidemiology Biomarkers & Prevention;2014-03
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