Trial-Ready in Days, Not Months
Zero-rejection regulatory packets. Automated readiness scoring. More time for patients, less time on paperwork.
Before and After Celina
Admin time
Packet prep time
An RFP just landed. You need to prove your site is trial-ready before the allocation decision. Your coordinators are already buried in compliance documentation.
This is the moment FQG+ scores your readiness.
Frequently Asked Questions
What is the current IRB/ethics committee rejection rate?
Every packet is verified against the jurisdiction's rule set before submission, with the applicable rule cited by name and version. We do not claim a rejection rate, because approval is the reviewing authority's decision, not ours. What we assemble is a packet with no preventable defects in it.
How much time do coordinators save?
Clinical research coordinators recover approximately 7.5 hours per week from automated compliance documentation, readiness scoring, and proactive regulatory monitoring. IRB packet preparation drops from 3-6 weeks to 3-5 days.
How does site readiness scoring work?
Celina evaluates site capability based on current documentation status, staff qualifications, equipment availability, patient population access, and regulatory compliance posture. This generates a predictive readiness score before sponsors commit activation budget.
What's the pricing model for site networks?
Site networks use per-site licensing that scales with network size. Volume tiers are available. Contact us for network-specific pricing based on your site count and jurisdiction requirements.
Can academic medical centers use TAI?
Yes. TAI includes governance workflows tailored to academic institutional review board structures, not forced into commercial templates. Co-creation and publication pathway collaboration are core to the academic engagement model.