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Featured Content

“Single IRB” vs “Central IRB” – What’s the Difference?
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“Single IRB” vs “Central IRB” – What’s the Difference?

With the rise of single IRB (sIRB) mandates, understanding the nuances between sIRB and central IRB (cIRB) is crucial for multisite studies.
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Beginner’s Guide to Clinical Trial Management Systems
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Beginner’s Guide to Clinical Trial Management Systems

From the largest research centers to the smallest, sites now recognize that a clinical trial management system (CTMS) can be configured to their needs and can bring powerful efficiencies insights, and compliance to their day-to-day operations.
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Beginner’s Guide to eTMF, eISF, and Regulatory Research Documents
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Beginner’s Guide to eTMF, eISF, and Regulatory Research Documents

Efficient document systems like eTMF and eISF enhance compliance and streamline document management, helping sites and sponsors ensure secure, organized trial records.
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Improving Study Activation Time for Gene Therapy Research
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Improving Study Activation Time for Gene Therapy Research

This blog explores how research sites are focusing on their institutional biosafety committee (IBC) programs as part of overall study activation time.
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