Build Grow Strengthen your registry
Guide your decision-making process with data you can count on. Clinical registries are a powerful tool that drive research, quality improvement, and the success of treatments, outcomes, and devices. Whatever your goal or specialty, Fivos provides both the infrastructure and the service necessary to develop and maintain a registry that illuminates trends and benchmarks physician best practices.
Move your registry into the future.
At Fivos, we guide societies, medical device companies, pharma, and health systems through the development of clinical registries to support value-based care and quality improvement initiatives for improved patient outcomes.
Built to spec
From concept to launch—our team runs with your ideas. With a true understanding of the registry design process, each client’s registry project is done to their specifications, with unprecedented turnaround time and deployment.
Real-time insights
Our scalable, secure, interoperable registry platform allows members to analyze real-time data and variability, and identify actionable improvements.
A registry resource like no other.
Long-Term Follow-Up
Long-Term Follow-Up
Dynamic Content
Dynamic Content
Extensive Service Offerings
Extensive Service Offerings
What our partners are saying
Registry Benefits
From outcomes analysis to resource utilization reduction, the benefits of registry participation are widespread.
- Firmly establish the credibility and support for a successful registry
- Foster meaningful participation from your physicians
- Enhance your reputation for member service and industry leadership
- Empower physicians to improve quality of care, reduce costs, and impact policy decisions
- Benchmark with medical societies at the regional and national level
- Support maintenance of certification for your physicians
- Support regional and national quality projects
- Access physician-level and center-level variation reports for peer review and sharing
- Utilize flexible, robust analytics to perform your own analyses, including those across health systems
- Determine longitudinal impact via follow-up reporting with life tables
- Mine and structure data to advance the understanding of devices and therapies, improve patient safety, and streamline development
- Facilitate seamless pre-market to post-market evaluation
- Supplement existing data with requested elements to expedite project completion, meet regulatory requirements, and reduce costs
- Collect necessary comparative device data as opposed to prospectively collecting this data over time
- Improve care through support and facilitation of quality initiatives and projects
- Identify meaningful benchmarks for QA and QI efforts
- Reduce expenses by addressing resource utilization, length of stay, and minimizing complications