The Power of Worldwide Networks in Data and Safety Monitoring Boards
In an era where clinical trials are increasingly global, it’s more imperative than ever to leverage international expertise. Data and
In an era where clinical trials are increasingly global, it’s more imperative than ever to leverage international expertise. Data and
Comprehensive IBC submissions require detailed materials, including investigator CVs, safety protocols, and site-specific SOPs for study agent handling.
The revised Common Rule introduces new exemptions, refined consent elements, and alters IRB oversight for multisite and minimal-risk research.
Navigate federal grant applications with Advarra’s expert checklist. Our streamlined process ensures compliance and participant protections for your research.
Advarra’s institutional review board (IRB) strives to protect participant rights and welfare throughout the research process.
DMC services Data monitoring committee (DMC) Independent DMC oversight supported by a 1500+ expert member network Advarra DMC services provide
More than four decades of ethical review leadership Advarra is the largest central IRB, pairing scale with deep scientific, regulatory,
REVIEWS IBC services Institutional biosafety committee (IBC) The fastest IBC timelines in the industry and more registered sites than any
REVIEWS CIRBI Platform Center for IRB Intelligence (CIRBI) Centralize and simplify IRB management with Advarra’s CIRBI platform. CIRBI enables faster
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
REVIEWS Frequently Asked Questions Find answers to our most frequently asked ethical review questions here. Can’t find what you need?
Antibiotic resistance is an emerging problem. Some have argued bacteria are developing antibiotic resistance faster than we can research, develop,