ABOUT ADVARRA
Advarra advances the way clinical research is conducted: bringing life sciences companies, CROs, research sites, investigators, and academia together at the intersection of safety, technology, and collaboration. With trusted IRB and IBC review solutions, innovative technologies, experienced consultants, and deep-seated connections across the industry, Advarra provides integrated solutions that safeguard trial participants, empower clinical sites, ensure compliance, and optimize research performance. Advarra is advancing clinical trials to make them safer, smarter, and faster. For more information, visit advarra.com.
BROCHURES
- Advarra Connect
- Advarra Cloud
- GxP Auditing, Compliance, And Specialized Consulting
- IRB Solutions To Empower Better Research Programs
- GMP Auditing, Compliance, And Specialized Consulting
- Clinical Quality Assurance And Compliance Oversight
- Streamline Data Collection, Management, And Compliance
- A Clinical Command Center For Efficient, Compliant Research
- Solutions For Health Authority Inspection Readiness And Remediation
- IRB Services For Institutional Sites
- Meeting Compliance Without Compromise
- Advarra University And Training
- Global Consulting Powered By Relevant Experience
- Mitigate Risk With Research Billing Compliance Services
- Cosmetics Research And IRB Review
- Advarra eReg Integrations Overview
- Successful Clinical Research Staffing Solutions
- Support For Institutions
- Advarra Custom Learning Portals
- Elevate Your Research With Comprehensive Tools And Expertise
CONTACT INFORMATION
Advarra
6940 Columbia Gateway Drive, Suite 110
Columbia, MD 21046
UNITED STATES
Phone: 410.884.2900
FEATURED ARTICLES
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This overview highlights real research programs at various stages of the recruitment process and demonstrates the impact of Advarra’s Longboat Platform across multiple therapeutic areas and sponsors.
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Learn why understanding the intricacies of IRB review for study changes is essential for researchers and institutions, covering everything from minor amendments to significant modifications, ensuring compliance and participant safety.
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Learn how a CRO was able to accelerate review times so COVID-19 vaccine trial sites could progress through site selection, IRB/IBC submission, approval, drug shipment, and complete site initiation visits in record time.
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By bringing objective evaluation, specialized expertise, and effective change management skills, learn how interim staff can significantly improve an institution’s ability to identify issues and implement necessary changes.
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With technology advancing clinical operations, proactive adaptation is paramount for organizations to remain at the forefront. How can your organization effectively navigate these evolving dynamics?
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Gain insight on how to prepare investigator site files (ISF) for audits and what teams should consider when looking to enhance efficiency and compliance.
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While training is beneficial, it's not universally required. The crucial aspect lies in ensuring that stakeholders understand the purpose of the training and whether it's the most effective solution.
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With Longboat, this pharma company trained all staff across trial sites, ensuring treatment for all 20,000 patients with real-time training reports.
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Creating new drugs or devices profoundly affects health and safety. See why it's vital for clinical research stakeholders — sponsors, CROs, and sites — to work together, meeting rigorous regulatory standards.
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Uncover how a biotechnology company experienced recruitment and compliance success after utilizing the Longboat Platform to provide training for every staff member at every trial site.
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Reporting noncompliance concerns is crucial to protect research participants. By promptly reporting noncompliance, researchers can ensure ethical research conduct and protect the rights and welfare of participants.
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By integrating independent Data Monitoring Committees into trial management processes, learn how sponsors can enhance trust, integrity, and the success of their clinical trials.
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Discover the strategic benefits of deploying consistent DSMB members across therapeutic programs, highlighting the pivotal role of program-level supervision in safeguarding the safety and effectiveness of novel treatments.
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Learn about strategies aimed to reduce protocol deviations and enhance compliance and quality. By implementing such measures, clinical trial teams can streamline operations and minimize the risk of regulatory issues.