Steps for a Successful Study Startup
Study startup is a critical stage in a clinical trial to get the study up and running. Efficient study startup lays an important foundation for the trial’s overall success.
CRO
2024 Site-Sponsor-CRO Collaboration Survey Report
The Site-Sponsor-CRO Collaboration Survey Report highlights challenges in collaboration, offering actionable insights from 200+ professionals to improve trials.
Data Monitoring Committee (DMC) Services
DMC services Data monitoring committee (DMC) Independent DMC oversight supported by a 1500+ expert member network Advarra DMC services provide
Institutional Review Board (IRB) Services
More than four decades of ethical review leadership Advarra is the largest central IRB, pairing scale with deep scientific, regulatory,
Institutional Biosafety Committee (IBC) Services
REVIEWS IBC services Institutional biosafety committee (IBC) The fastest IBC timelines in the industry and more registered sites than any
From Simulation to Success: Stress Testing Your Inspection Readiness
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Oncology Clinical Research
SOLUTIONS FOR Oncology Clinical Research As a cancer research leader, you face unique challenges requiring specialized support and expertise. Whether
Reviews FAQ
REVIEWS Frequently Asked Questions Find answers to our most frequently asked ethical review questions here. Can’t find what you need?
Review Services
REVIEWS Comprehensive Global Review Services Ensure comprehensive ethics and safety oversight with Advarra’s full suite of ethical review committee services.
Clinical Research Training Solutions
Clinical research training solutions Advarra provides engaging and innovative training solutions to ensure your team is prepared for research in
Single IRB Review: Tips for Sponsors and CROs Working with Institutional Sites
Discover strategies for sponsors and CROs to navigate single IRB mandates, from institutional IRB roles to optimizing compliance and efficiency.
CAR T Manufacturing and Toxicity
CAR T Manufacturing and Toxicity Pre-Clinical Considerations Genetically engineered therapeutics present diverse, and sometimes heightened, risks compared to traditional small