The Ethics of Mandatory Retention of Clinical Biospecimens for Research-Reference-Cited by-同舟云学术

The Ethics of Mandatory Retention of Clinical Biospecimens for Research

Published:2021-01-26 Issue:9 Volume:36 Page:2818-2819
ISSN:0884-8734
Container-title:Journal of General Internal Medicine
language:en
Short-container-title:J GEN INTERN MED

Author:

Wendler David^ORCID

Funder

National Institutes of Health

Publisher

Springer Science and Business Media LLC

Subject

Internal Medicine

Link

https://link.springer.com/content/pdf/10.1007/s11606-020-06468-9.pdf

Reference7 articles.

1. SACHRP. Attachment C - Updated FAQs on Informed Consent for Use of Biospecimens and Data. Available at: https://www.hhs.gov/ohrp/sachrp-committee/recommendations/attachment-c-faqs-recommendations-and-glossary-informed-consent-and-research-use-of-biospecimens-and-associated-data/index.html.

2. Wolinetz CD, Collins FS. Recognition of research participants’ need for autonomy remembering the legacy of Henrietta Lacks [Published online August 11, 2020]. JAMA. https://doi.org/10.1001/jama.2020.15936.

3. Wendler D. Are physicians obligated always to act in the patient’s best interests? J Med Ethic. 2010;36:66–70.

4. Edwards KL, et al. Genetics researchers’ and IRB professionals’ attitudes toward genetic research review: a comparative analysis. Genet Med. 2012;14:236–42.

5. Wendler D, Rid A. Genetic research on biospecimens poses minimal risk. Trends Genet. 2015;31:11-5.

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ethics in laboratory medicine: an African perspective;The Journal of Medical Laboratory Science and Technology of South Africa;2023-12