Phuse US 2024 – Booth demos
Book a Free Demo of Pinnacle 21 Clinical Study Software Suite at Phuse US Connect 24
If you’re here it means you’re interested in finding a quicker, easier way to build and submit high quality trials…
So submit this form to book your no-obligation live demo at Phuse, and see how much quicker you could go from protocol to submission!
Just tell us what day/time suits you in the message box, and one of our team will be in touch with you to confirm:
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How you’re better off with Pinnacle 21
Start trials in less than half
the time
Build validated studies in less than 6 weeks by standardizing and reusing approved study content. With faster study setup and earlier enrolment, lifesaving drugs can be brought to market sooner.
Earlier informed
decisions
Get real-time SDTM data from first patient in (FPI), and make informed safety and efficacy decisions, earlier, with on-demand insights.
Superior data
quality
Ensure the quality and integrity of clinical trial data with real-time validation, issue management and resolution.
Improve
compliance
Ensure regulatory compliance and accelerate submission readiness with data quality control, CDISC conformance, and fitness-for-use reports.
Maximize chances of submission approval
Pre-approved, standardized content and built-in validation puts you in the strongest position for gaining FDA approval.
Reduce costs
& maximize profits
Save labor, time, and costs as manual work is replaced by automated processes. Now you can increase productivity, as skilled resources can be diverted to more profitable projects.
What people say about us
Pinnacle 21 and Formedix have joined forces!
Our unified platform will improve collaboration and data flow across key stakeholders, whilst enabling faster, higher quality trials, from design to submission.