Study Activation Consulting
Make your clinical trial operations more competitive and your study activation process more efficient with a comprehensive assessment, best practices guidance, and implementation support from Advarra.
A successful institutional research program depends on a reliable and well-functioning clinical operations department and IRB. With IRB and research technology experts ready to hit the ground running on-site or ...
Research Administration Consulting
Strong research administration infrastructure is critical for success in today’s changing regulatory and business climate. Advarra Consulting helps you to address the challenges of discovery science, translational research, and clinical ...
Insights Info Sheet
Advarra’s business intelligence solution provides turnkey, intuitive dashboards that deliver meaningful insights, with in-depth analysis of past performance, current state, and projected outcomes.
Advarra EDC Implementation and Validation Services Overview
Leverage Advarra’s robust implementation and validation process.
A completely managed service to navigate regulatory risks and increase the capacity of your local IRB office. Advarra GPS™ helps guide you through compliance risks, protect you from staffing challenges, ...
GMP Consulting Services Menu
Advarra helps clients minimize risk and maintain compliance with good manufacturing practice (GMP), good laboratory practive (GLP), and good tissue practice
Budget Setup Service Info Sheet
Expedite your OnCore implementation and study activation processes, and allow your staff to focus on high-value tasks more closely tied to your research.
Central Neurology Review Services
With extensive experience in neurology research and clinical care, Advarra’s Central Neurology Review (CNR) provides the robust human subject protections review that research institutions prefer.
EVAL Info Sheet
Showcase the impact of your research to the NCI, NIH, and to your organizational leadership.
IBC Review and Consulting Services
No more waiting for a standing meeting. No submission deadlines. Responsive and flexible—only 10 business days or less from submission to institutional biosafety committee (IBC) review.
Advarra Consulting Global Services
With clinical QA staff and qualified consultants located around the world, Advarra Consulting has experience performing audits in numerous countries.