| Literature DB >> 27558027 |
A W Warner1, H Moore2, D Reinhard3, L A Ball4, B M Knoppers5.
Abstract
One of the many challenges of translational medicine is working with research participants to donate biospecimens through an ethical informed consent framework. The increasingly complex ethical and regulatory differences across jurisdictions translates into limitations on use and potential value of biological specimens and their associated data in clinical research. We introduce a call to action for more uniform global standards for collection of biological specimen informed consent data to enable greater advancements in medical research.Entities:
Mesh:
Year: 2016 PMID: 27558027 DOI: 10.1002/cpt.461
Source DB: PubMed Journal: Clin Pharmacol Ther ISSN: 0009-9236 Impact factor: 6.875