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
Rejection rate
Admin time
Packet prep time
Frequently Asked Questions
What is the current IRB/ethics committee rejection rate?
Industry average first-submission rejection rate is 25-30%. With NexTrial's zero-rejection architecture, rejection rates drop below 5% by validating packets against jurisdiction-specific requirements before submission.
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.