Actionable Clinical Trial Data Visualizations

See the Difference with our Expertise

• Enhanced Decision-Making

  Our tailored Key Risk Indicator (KRI) dashboards provide real-time insights, allowing you to identify and quantify risks promptly. This proactive approach helps prevent trial disruptions and ensures compliance with regulatory standards. By visualizing critical metrics such as screen failure rates, adverse events (AEs), serious adverse events (SAEs), and query rates, you can detect potential issues early and take corrective actions before they escalate.

• Comprehensive Site Metrics Monitoring

  The performance and compliance of each clinical trial site is essential for maintaining data quality, patient safety, and operational efficiency. Veranex's site metrics trackers offer a detailed view of site activities, helping you ensure that all sites adhere to database lock timelines and other critical milestones. This level of oversight is particularly beneficial under risk-based monitoring frameworks, where timely and effective clinical monitoring is paramount.

• Clean Patient Tracker (CPT)

  Ensure data readiness for analysis and accelerates database lock timelines. By prioritizing sites that are lagging in queries and source data verification (SDV) issues, the CPT helps streamline your trial processes and enhances overall efficiency. This tool is invaluable for keeping your trial on track and ensuring that your data is always ready for analysis.

• Global Talent and Expertise

  At Veranex, we leverage a global pool of talent and advanced analytics to provide you with the best data visualization solutions. Our team of experts is well-versed in medtech trials and understands the unique challenges and requirements of the industry. This expertise ensures that our visualizations not only meet regulatory requirements but also maintain the integrity of your study, fostering trust and confidence in your results.

• Sophisticated Alerts

  Safer Trials Safety is a top priority in medical device trials. Veranex's high-end sophisticated alerts for adverse events (AEs) and serious adverse events (SAEs) ensure that you are always aware of any potential safety issues. These alerts enable you to take immediate action, ensuring the highest standards of patient safety and trial quality.

• End-to-End Dashboard Development

  We offer comprehensive development of clinical trial dashboards, from initial design to final implementation. Our end-to-end approach ensures that your dashboards are tailored to your specific needs and provide the insights you need to drive impactful results. By using reusable templates, we can deliver dashboards quickly and efficiently, saving you time and resources.