Reporting Requirements
Let’s Get Ethical
Advarra's IRB Chairs Luke Gelinas and Amanda Higley discuss hot topics in clinical research, including cannabis studies and data ownership.
A Look at the Processes Behind Clinical Endpoint and Event Adjudication
Take a closer look at how and why we leverage proprietary, custom, and intelligent technology in our EAC program
Top-Tier University Stays Compliant with Advarra’s HRPP Assessment
A top -tier university worked with Advarra’s Institutional Research Center of Excellence to assess HRPP compliance with federal regulations
Why Device, Diagnostic, and Digital Therapeutic Research Needs Endpoint Adjudication
This blog outlines when a device clinical trial sponsor should engage an EAC or CEC to provide specific medical expertise & safety oversight.
IRB Services for Federal Grants
View this info sheet to learn about Advarra’s IRB expert oversight and guidance to support your next federal grant proposal.
Considerations for IRB Review: Artificial Intelligence & Machine Learning
Read this blog to learn IRB review considerations for artificial intelligence and machine learning studies.
DMC vs EAC: What’s the Difference?
This blog outlines the requirements for each committee, what it does, and the critical roles each plays in keeping research participants safe.
Beginner’s Guide to Clinical Trial Billing Compliance
Ensuring proper compliance within clinical trials is confusing, so here are best practices to ensure charges and claims are correctly routed
Local Versus Central IRBs: What’s the Difference?
Local IRBs and central IRBs are not really that different, although sIRB mandates have complicated things for local IRBs.
What Level of Review Does Your Study Need?
In this infographic, we share useful information for investigators to know which level of IRB review likely applies to their study.
Keys to Advancing Your Biotech Go-to-Market Plan
Essential keys for growing biotech companies on navigating the complexities of the FDA 510K filing process.
Beginner’s Guide to Clinical Trial Management Systems
A clinical trial management system (CTMS) can bring powerful efficiencies, insights, and compliance to sites' day-to-day operations.
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