If you are a researcher doing investigator-initiated studies or trials – we can help. The Celéri Research Group will assist you with optimal study design to achieve your protocol’s objectives while ensuring fast study readiness. Through our robust electronic data capture, you can collect study participant data via electronic Case Report Forms (eCRF), clinical logs and integrations with wearables, smart scales, etc. Most importantly, we are experts in electronic Patient Reported Outcome (ePRO) development. Use our existing library of already available PRO assessments or we can assist you with custom design of questionnaires tailored for your study’s needs. Finally, we bring a dedicated network of pain provider sites to the table.
If you are a Sponsor, we offer post-market studies for the advanced support of your device or therapeutic. Our depth of clinical registry experience allows us to gives you the irrefutable data and insights you need so you can be confident in meeting RWD requirements.
We integrate with several of the leading EMRs with more in process. Come talk to us about integrating our Real World Outcomes seamlessly into your practice workflow.
Data is gathered using the Celéri Tablet’s proprietary software system that allows data collection in-clinic or from a patient remotely using their own device.