5 Considerations for Evaluating an eIRB System
In addition to other responsibilities, human subjects protection programs (HRPPs) and IRBs are tasked...
FEATURED E-BOOK
Making Good Clinical Practice More Understandable
This eBook dives into GCP’s role in the clinical research ecosystem and how it protects participant rights, safety, and confidentiality.
The Powerful Potential of Open Collaboration
Advarra’s Site-Sponsor Consortium emphasizes shared standards and transparent dialogue, paving the way for scalable,...
Reuniting and Reconnecting at the 2022 Onsemble Conference
Throughout the day on Tuesday, March 29, clinical research professionals arrived at the Westin...
mRNA Clinical Trials: Key Regulatory Considerations
Over the past two years, Operation Warp Speed brought mRNA-based vaccines into the spotlight,...
Clinical Endpoint Adjudication Committees: Not Just for “Endpoints”
This blog outlines some of the critical events where endpoint adjudication committees (EACs) can...
A Look at the Processes Behind Clinical Endpoint and Event Adjudication
See how Advarra’s tech-enabled adjudication platform leverages expert collaboration and secure data integration to...
A Journey in Support of Diversity
Since he was young, Sergio Armani has always found solace on the bike, spending...
The Impact of Digital Transformation in Clinical Trials
Digital transformation. We’ve heard about it for years, but now all of us have...
Why Device, Diagnostic, and Digital Therapeutic Research Needs Endpoint Adjudication
In its March 2006 guidance, Establishment and Operations of Clinical Trial Data Monitoring Committees,...
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