If you are a researcher exploring investigator-initiated research, studies or trials – we can help.  The Celéri Health 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 site management to the table with ready site access to over 350 pain network providers and AI-based patient recruitment capabilities.

If you are a Sponsor, we offer a full range of trials….IDE to post-market studies… for the advanced support of your device or therapeutic.

Our depth of clinical registry experience allows us to give you the irrefutable data and insights you need so you can be confident in meeting RWD requirements.

The fact that we have a ready-consortium of partners in our Research Group allows you to customize your contract to include only the services needed:

• Full service CRO Partners (fit to your purpose with a smaller firm or a larger one)
• Biostatistics
• KOLs
• Medical Writing
• Regulatory Consultants
• Site Monitors
• Robust Data Management
• EDC Vendors (small, medium and large