Recent court decisions could make it more difficult for scientists to individually secure usage rights for research involving the study of human biological materials, as patients and clinicians have begun to question exactly what is granted—and to whom it is granted—when a patient signs an informed consent agreement.
Read the complete article by clicking on the link below.
Related Insights
March 9, 2026
Foley Viewpoints
Using Loan Regime Split-Dollar Life Insurance to Navigate Nonprofit Executive Compensation Rules
A loan regime split-dollar life insurance arrangement can be an important option to provide retirement benefits to nonprofit executives…
March 9, 2026
Foley Viewpoints
New Markets Tax Credit Financing: Subsidy for Health Care Facilities and Operations
Enacted 25 years ago, the federal New Markets Tax Credit (NMTC) Program has become a powerful financing tool for health care…
March 9, 2026
Energy Current
Dept of Interior Proposes Revisions to Rules Licensing Producers of Governing Offshore O&G
On March 5, 2026, the Dept. of the Interior, acting through the Bureau of Ocean Energy Management (BOEM) issued a pre-publication copy of…