CLINICAL RESEARCH SITES
Solutions Built for Sites
Advarra’s intuitive technologies and services solve your day-to-day challenges so you can focus on your most important stakeholders – patients.
Trusted by Sites Everywhere
Advarra Connects Every Phase
of Your Clinical Trial
Planning
- Streamline review Submission
- Identify sites and activate studies
- Ensure site feasibility and compliance
Start-up
- Review and transfer documents securely
- Establish budgets and timelines
- Train sites to maximize efficiency
Study Conduct
- Organize documents & track amendments
- Provide positive patient experiences
- Manage research operations
- Learn from the Onsemble Community
Close Study
- Measure success & identify improvements
- Manage stipends & reimbursements
Built to Meet Site’s Top Needs
Better Bill Compliance
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Faster Study Startup
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Simplified Data Management
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Engineer Mike Wallace
Explains Why Advarra is an Industry Leader in Security and Compliance
Children’s Hospital Expedites Study Process with Advarra’s Professional Services
Biotech Organization Partners with Advarra to Become Inspection Ready
Site Streamlines Operations with Advarra EDC Study Design Service
Developing an Enterprise Roadmap to Post Authorization Safety Studies
UNPARALLELED EXPERTISE
Advarra Knows Security and Compliance
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Collaborate and Drive Clinical Research Forward
Join a robust network of the nation’s leading clinical research professionals to share best practices, addressing current challenges, and shape the industry.
