Advarra Launches Study Design Solution, Powered by Braid, to Improve Operational Efficiency in Clinical Trials — Read the Press Release

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How to Optimize Your sIRB Experience

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.

Your Guide to sIRB Mandates

In the past few years, new regulations and policies have been announced and implemented to address the challenges of conducting clinical trials involving multiple research sites. Chief among these requirements is the use of a designated sIRB for multisite research.

IRB and HRPP Advisory Services

STRATEGIC ENABLEMENT SERVICES HRPP/IRB Advisory Services Advarra’s Human Research Protection Program (HRPP)/Institutional Review Board (IRB) Advisory services include accreditation support,

Not if, but When: A Study Manager’s Guide to Adaptability and Incoming Trends

Our webinar discusses key near-term trends and regulations and investigate persistent challenges frequently throwing even the most efficient teams off track. Advarra and industry representatives will dive deeper into achieving critical milestones across study startup, conduct, and close out that every project manager should optimize.

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