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.

More:

• All of our study-collected data can be coupled with use of Consolidated-Clinical Document Architecture (C-CDA) data from your EMR, which decreases administrative burden on your staff – and offers a more robust clinical dataset.
• Once your study starts enrolling, you will 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.

Talk to our research team.