Advarra GPS
Advarra’s IRB support services help institutions streamline research while leveraging the world’s largest integrated IRB processes and technology.
2024 Site-Sponsor-CRO Collaboration Survey Report
The Site-Sponsor-CRO Collaboration Survey Report highlights challenges in collaboration, offering actionable insights from 200+ professionals to improve trials.
Materials Required for Submitting a Study to the IBC
Comprehensive IBC submissions require detailed materials, including investigator CVs, safety protocols, and site-specific SOPs for study agent handling.
Revised Common Rule Reference Guide
The revised Common Rule introduces new exemptions, refined consent elements, and alters IRB oversight for multisite and minimal-risk research.
IRB Information for Participants and Patient Advocacy Groups
Advarra’s institutional review board (IRB) strives to protect participant rights and welfare throughout the research process.
Empowering Clinical Trials: The Pivotal Role of eSource
Discover how eSource platforms revolutionize clinical trials by simplifying data collection and ensuring accuracy, accessibility, and reliability.
Adapting to the Evolving Era of Oncology: Implications and Strategies for Research Institutions
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Building Buy-in: Strategic Training for Clinical Research Success
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
From Simulation to Success: Stress Testing Your Inspection Readiness
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Decentralized Clinical Trials Involving Biologics: Unique Challenges
Join this webinar to learn about FDA insights on DCTs and biologics. Dr. Eisenman discusses biosafety, risks, and key considerations for safe trials.
Medicare Coverage Analysis in Oncology Trials
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Preparing Your Action Plan for the FDA sIRB Mandate
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.