September 26, 2016
NIH has developed a one-page guide to explain how to address rigor and reproducibility in your NIH application.
September 26, 2016
Beginning with the January 25, 2017 application due date, NIH will change what post-submission materials are allowable.
September 27, 2016
NIH has recently released its policy on the use of a single Institutional Review Board (sIRB) for multi-site research.
September 26, 2016
A recently published finding from investigations by federal regulators [Human Res Rept, Sep. 2016, 31(9), 9]:
The U.S. Food & Drug Administration (FDA) found that a physician-investigator conducting two GlaxoSmith-Kline multisite studies of
September 26, 2016
The Food and Drug Administration (FDA), in collaboration with the University of Maryland Center of Excellence in Regulatory Science and Innovation (M-CERSI), is announcing a 3-day training course for clinical investigators on the scientific, ethical, and regulatory aspects of clinical trials for medical products.
September 26, 2016
Funding opportunities available to our investigators.
September 26, 2016
New NIH electronic processes that will be available starting in 2017.
September 26, 2016
NIH now allows applications to be withdrawn electronically through the NIH Commons.
