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.
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Single IRB (sIRB) review streamlines oversight for multisite trials, reducing administrative burdens while ensuring participant protections across all sites.
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
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.
On September 28, 2022, the Food and Drug Administration (FDA) released two proposed rules, or Notices of Proposed Rule Making
STRATEGIC ENABLEMENT SERVICES HRPP/IRB Advisory Services Advarra’s Human Research Protection Program (HRPP)/Institutional Review Board (IRB) Advisory services include accreditation support,
Advarra Innovation Summit Cambridge, MA June 11, 2025 | 8:30 am – 5:00 pm ETLe Méridien Boston Cambridge Explore the
At a busy research site, a clinical trial is ready to launch — but it’s stuck in limbo over a
Our webinar discusses key near-term trends and regulations and investigate persistent challenges frequently throwing even the most efficient teams off track. Advarra and industry representatives will dive deeper into achieving critical milestones across study startup, conduct, and close out that every project manager should optimize.
2024 has been a year of growth and evolution in clinical research. The coming year is expected to be no