NIH sIRB Docs Contact Us
Simplify your grant application with sIRB support documents tailored to meet requirements for NIH and other federally funded multisite research.
Simplify your grant application with sIRB support documents tailored to meet requirements for NIH and other federally funded multisite research.
As the research community’s preferred sIRB partner, we help you meet regulatory requirements with efficiency and transparency.
James Riddle outlines the impact of the anticipated sIRB mandate, and argues how this is an opportunity for sponsors to
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Implementing an sIRB process requires addressing unique local considerations, from consent requirements to cultural nuances, ensuring a streamlined yet ethical review process.
As sIRB mandates reshape the clinical trial landscape, study teams must navigate unique challenges while ensuring compliance and participant protection.
Once the FDA’s sIRB mandate is in effect, it will affect the remainder of non-federally funded research, and then nearly all multisite research conducted in the US will require sIRB review.
Got questions about sIRBs? Join experts as they share insights and priorities, plus a Q&A to address common concerns and your live questions.
Prepare for single IRB review with insights on reliance agreements, communication plans, lead site responsibilities, and technology needs.
HRPP staffing is essential for maintaining research ethics, even with sIRB mandates streamlining review processes for multisite studies. Discover key HRPP roles and benefits.