Elevate Your Research
Advarra offers comprehensive services designed to streamline your study activation and research productivity. Maximize your investment through breakthrough efficiencies with our technology solutions and research services.Start the Conversation
Institutional Review Board (IRB) Services
IRB solutions to safeguard trial participants
Manage regulatory requirements, simplify reporting, and monitor review status in real time.
Over 3,500 institutions, hospitals, health systems, and academic medical centers (AMCs) trust Advarra to ensure compliant research conduct for everything from single investigational sites to multiple site research consortia and therapeutic networks.
Institutional Biosafety Committee (IBC) Services
Comprehensive review and oversight of clinical trials involving investigational products containing engineered genetic material
Is your site prepared to conduct gene therapy and mRNA-engineered vaccine research? Join the world’s largest Gene Therapy Ready site network and save 5-6 weeks off your study activation timeline.
Alleviate Your Administrative Burden with Advarra’s Professional Services
Increase your research productivity, maximize your Advarra investment, and experience breakthrough efficiencies with our technology-enabled professional services.
- Coverage Analysis: Ensure your site stays compliant with Medicare billing compliance
- Budget Negotiation: Accelerate your timeline, alleviate budget negotiation burdens, and ensure your funding goals
- Custom eLearning: Ensure consistent and accurate training
- Informed Consent Development: Guarantee clinical trial documentation is compliant and easily understandable
- Protocol Calendars: Expedite study activation with custom clinical trial management system (CTMS) calendars
- Research Staffing Solutions: Engage top-level professionals to fill core team roles
- EDC Study Design: Accelerate IIT portfolio with high-quality calendars and forms
- Budget Setup: Improve implementation and timelines, enabling Advarra to manage finance-related data entry
- Study Activation Consulting: Receive the necessary expertise, and technology solutions to improve timelines
Institutional Research Center of Excellence
Consulting services for today’s research-intensive universities, academic medical centers, and sites
- Research Compliance: Ensure regulatory compliance within clinical research programs
- Research Administration: Streamline and fortify the research architecture of your health system
- Research Operations: Site-level assistance with clinical trial operations
- HRPP/IRB Consulting Services: Significant expertise in the implementation of compliant human research protection programs
Making the Most of Site Training: Lessons from the Pandemic
The investigator meeting and site initiation visit (SIV) are two critical milestones marking the beginning of a clinical trial for...
Ensure that your next remote site initiation visit is both productive and useful despite the virtual setting with these tips
Improving Study Activation Time for Gene Therapy Research
Gene therapies and genetically engineered vaccines are growing exponentially and will continue to become more popular. Per a report from...
With the growing popularity of gene therapy research and genetically engineered vaccines, sites need to understand study activation impacts
Q&A – Regulatory Fine Points: Exploring 21 CFR Part 11 Validation
In a recent webinar, James Riddle, Shannon Roznoski, and Stuart Cotter of Advarra presented Regulatory Fine Points: Exploring 21 CFR Part...
Advarra's experts answer audience questions from our Regulatory Fine Points: Exploring 21 CFR Part 11 Validation webinar.