Don’t just run a registry.
Run a real-time study that accelerates access, expands labels, and fuels product innovation.
Celéri transforms your registry into a regulatory-grade, real-time evidence engine—designed for speed, credibility, and payer alignment.
MedTech and Pharma companies are under pressure to demonstrate real‑world value faster than ever. Traditional registries are static and slow.
Celéri’s approach goes further – we design real‑time studies that capture longitudinal patient outcomes, integrate seamlessly into clinical workflows, and deliver insights powerful enough for FDA and payer submissions.
Capture Data
Integrate
Analyze
Submit
Real-Time Studies
- Regulatory-ready evidence aligned with FDA and EMA standards
- Access to >250 pain physicians in our Research Network
- Integrated patient-reported outcomes (PROMIS, PHQ-9, GAD-7, ODI, etc.)
- Streamlined operations with our EDC + Data Management platform
Breakthrough Designation
Preparing for a breakthrough designation? Celéri empowers you with evidence for accelerated regulatory review.
Label
Expansion
Expanding your label?
Get the longitudinal data you need for regulatory and promotional confidence
Post‑Market
Adoption
Driving post‑market adoption? Generate real‑world insights for payer and clinician endorsement.
Our Studies Support FDA And Payer Submissions.
Celéri’s regulatory experts design studies aligned with FDA and EMA standards, ensuring your evidence is credible and submission-ready. We help you generate the real-world data payers and regulators need to accelerate approvals and coverage decisions.
