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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.
Research-Ready Training
Activate new sites and investigators efficiently with effective, engaging, and efficient training on introductory research and conduct essentials with our Research-Ready training.
Q&A Part 1 – Gene Therapy Research in the Age of COVID-19
Panelists from Advarra’s inaugural virtual symposium participated in a Q&A session to address questions submitted by the audience. Read part 1:
NIH 2023 Data Management and Sharing Policy: What you Need to Know
Optimizing Your Data Management Plan: Best Practices for Biomedical Research under the NIH Data Sharing Policy
Sickle Cell Disease: The Importance of Amplifying Patient Voices
Sickle cell disease significantly impacts the African American population, a minority community historically underserved by clinical research.
Staying Connected and Compliant: Reimagining Clinical Trials with Longboat
Learn how Longboat is reimagining critical workflows across sites, sponsors, CROs, and patients.
The Importance of Strategic Planning for Long-term Training Success
Explore key strategic planning actions to foster a proactive mindset when designing training and documentation.
Beginner’s Guide to Independent Asset Reviews
Learn more about independent asset reviews and how they can enhance research operations.
Reuniting and Reconnecting at the 2022 Onsemble Conference
The 2022 Onsemble Conference provided an opportunity for attendees to reconnect in person and collaborate to move research forward.
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