sIRB 101: An Introduction to Relying on an External IRB
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Search Results for: sirb
What is an sIRB and Why Does my Study Need One?
Single IRB (sIRB) review streamlines oversight for multisite trials, reducing administrative burdens while ensuring participant protections across all sites.
How to Optimize Your sIRB Experience
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Your Guide to sIRB Mandates
In the past few years, new regulations and policies have been announced and implemented to address the challenges of conducting clinical trials involving multiple research sites. Chief among these requirements is the use of a designated sIRB for multisite research.
FDA Proposes Revised IRB Regulations, Including Required sIRB for Multisite Trials
On September 28, 2022, the Food and Drug Administration (FDA) released two proposed rules, or Notices of Proposed Rule Making
IRB and HRPP Advisory Services
STRATEGIC ENABLEMENT SERVICES HRPP/IRB Advisory Services Advarra’s Human Research Protection Program (HRPP)/Institutional Review Board (IRB) Advisory services include accreditation support,
Advarra Trust Center
Welcome to Advarra’s Trust Center At Advarra, trust is the cornerstone of our relationships with clients, employees, and partners. Our
Advarra Innovation Summit | Cambridge, MA
Advarra Innovation Summit Cambridge, MA June 11, 2025 | 8:30 am – 5:00 pm ETLe Méridien Boston Cambridge Explore the
Ways to Streamline Informed Consent Process in Clinical Trial Startup
At a busy research site, a clinical trial is ready to launch — but it’s stuck in limbo over a