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Posted Date

November 20, 2013

Biobanking: When Issues with Tissues Come a’Knockin’

Carol J. Weil, from the National Cancer Institute, and former OHRP staff, Samantha Smith, discuss ethical and regulatory issues involving the collection, storage, and research use of biospecimens including, informed consent frameworks, privacy concerns, the identifiability, models for data sharing, and return of research results.

CE: 1:00 CIP Unit (OHRP doesn't provide documentation but viewers can provide the date, time, title, and URL on the CIP recertification application.)

Note: This video was created before the 2018 revisions of the Common Rule and may include information that is not up to date.

Clinical Trials
Common Rule
FDA
HIPAA
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