Why Now is the Right Time to Adopt eConsent
eConsent streamlines trial participation, allowing remote access and minimizing paperwork errors, benefitting both research staff and participants alike.
Technology
Analyzing 1,000+ Study Startup Records for Recruitment Performance with Advarra Study Collaboration solutions
Our team investigated Advarra study collaboration solutions (Advarra Study Startup and Advarra Enroll) impact on site’s ability to reach recruitment goals on time – regardless of sponsor or therapeutic area. Download the case study to learn more.
Top Biotech Achieves Recruitment and Improves Compliance Across 30 Sites
Download the case study to find out how the Advarra’s study collaboration solutions ensured not only recruitment success, but site and participant support and compliance.
Yale Enhances Patient Safety, Billing Workflows with OnCore and EMR Integration
Discover how Yale, Advarra, and Epic improved billing compliance, streamlined workflows, and enhanced participant safety through OnCore-EMR integration.
Modernizing Site Feasibility and Selection
Study startup is a complicated, multi-faceted process – notoriously prone to delays due to the many stakeholders, systems, and decisions
Unpacking IRB Innovations for Decentralized Clinical Trials
In the blink of an eye, the world has gone digital. So many tasks which used to require going to
How Paper and Electronic Source Data Meet ALCOA-C Principles
According to the FDA, data should meet certain fundamental elements of quality (ALCOA), whether they’re recorded on paper or electronically.
Strategies for Successful Site Selection in Clinical Trials
Clinical trial site selection can make or break a trial’s success before it even begins. The average cost to open
Keys to Unblocking the Innovation Bottleneck in Research
Is the clinical research industry winning or failing at innovation? It probably depends on who you ask and likely full
Streamline Study Startup with Improved Site Selection & Feasibility
Site selection for clinical trials is often one of the biggest headaches for pharmaceutical sponsors and contract research organizations (CROs).
Beginner’s Guide to 21 CFR Part 11 Compliance
Ensuring 21 CFR Part 11 compliance in research software protects data integrity, security, and audit trails, essential for meeting FDA electronic documentation standards.
Regulatory and Ethical Considerations for eConsent in Research
IRB oversight, identity verification, and comprehension checks are critical in eConsent, ensuring ethical and legal standards while improving participant understanding.