improve study quality
and optimize RWE data.
If you are a researcher doing investigator-initiated studies or trials – we can help. The Celéri Team of research professionals will assist you with optimal database design to achieve your protocol’s objectives while ensuring fast study readiness. Through our Multichannel High-Resolution 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. Patients can complete their PRO questionnaire assessments in clinic on a tablet or on their own device via SMS/email. In addition, PRO assessment sending can be automated based on a pre-determined cadence following a therapeutic intervention.
These study-collected data can be coupled with our use of Consolidated-Clinical Document Architecture (C-CDA) data from your EMR for a robust clinical dataset, which decreases administrative burden on your staff.
Once your study starts enrolling, you will always have on-demand/real time access to your study results in order to ensure real time data currency/accuracy and to perform data analytics. Most importantly, your clinical study data can be compared against other similar therapies within our vast commercial database.
And once your clinical study ends, use the Celéri platform commercially to continue to obtain PRO and EMR information for former clinical study participants long after study completion.
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.
using our data
