Projects/packages requiring Full Committee Review must be determined to be complete before these are placed on the agenda for review at a scheduled IRB meeting. Project/packages requiring ...

Before a clinical trial can begin, the protocol must be approved by UCSF's Institutional Review Board. After a clinical trial is approved by the IRB, a UCSF team of researchers, clinicians and other ...

The Smith College Institutional Review Board (IRB) upholds the principles of respect, beneficence and justice, with established guidelines to ensure that human research participants are treated with ...

Ainos (AIMD) announced progress in advancing its oral interferon drug platform, VELDONA in the rare disease space. The Taiwan Food and Drug ...

Dual Trials Accelerate VELDONA® Toward Rare Disease Market Entry Bridging Strategy Aims to Fast-Track U.S. Regulatory Approvals SAN DIEGO, CALIFORNIA / ACCESS Newswire / April 14, 2025 / Ainos, Inc.

If you plan to conduct research on human subjects, you will need to work with CU Boulder’s Institutional Review Board (IRB). The purpose of the IRB is to help ensure that human subject research is ...