Human Research Protection Program Services
Advarra knows that one size does not fit all. Each research program is different, with unique needs and distinct personalities. We take time to carefully understand your process and then…
Coverage Analysis Services
Ensure your site stays in compliance with Medicare billing compliance regulations with industry standard methods combined with national and regional coverage determinations and proprietary solutions.
GxP Auditing, Compliance, and Specialized Consulting
Advarra’s experts can work directly with your team to provide consulting and evaluation services related to GCP, GMP, GLP, GVP, GDP, and quality assurance (QA).
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.
Staff Augmentation
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…
Advarra GPS™
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
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.
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.