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Improve diversity and inclusion in clinical research with Advarra’s global expertise in DE&I planning and recruitment strategy development.
Improve diversity and inclusion in clinical research with Advarra’s global expertise in DE&I planning and recruitment strategy development.
Optimize study startup and execution with Advarra’s integrated solutions, including IRB/IBC reviews, consulting, and regulatory expertise.
Save time with Advarra Connect, reducing effort by up to 15 minutes per document routed to your eTMF within a connected research ecosystem.
Advarra’s IRB support services help institutions streamline research while leveraging the world’s largest integrated IRB processes and technology.
The Site-Sponsor-CRO Collaboration Survey Report highlights challenges in collaboration, offering actionable insights from 200+ professionals to improve trials.
Comprehensive IBC submissions require detailed materials, including investigator CVs, safety protocols, and site-specific SOPs for study agent handling.
The revised Common Rule introduces new exemptions, refined consent elements, and alters IRB oversight for multisite and minimal-risk research.
Advarra’s institutional review board (IRB) strives to protect participant rights and welfare throughout the research process.
Discover how eSource platforms revolutionize clinical trials by simplifying data collection and ensuring accuracy, accessibility, and reliability.
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.