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Advarra Single Sign-On (SSO) for user authentication allows users to access all SSO-enabled Advarra products…

Study startup is a critical stage in a clinical trial to get the study up…

Comprehensive IBC submissions require detailed materials, including investigator CVs, safety protocols, and site-specific SOPs for…

The revised Common Rule introduces new exemptions, refined consent elements, and alters IRB oversight for…

Advarra’s institutional review board (IRB) strives to protect participant rights and welfare throughout the research…

Learn the essentials of institutional biosafety committees (IBCs), their role in research, and how they…

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