Let our clinical metadata repository transform your clinical data into high-quality, submission-ready deliverables. By combining metadata management and continuous data validation in a collaborative platform, you’ll accelerate timelines, reduce the risk of costly delays, and ensure end-to-end compliance.
Pinnacle 21®
Personalized demo of Pinnacle 21 clinical data standardization software
Reduce timelines with increased quality & automation from setup through submission
With Pinnacle 21 Enterprise you get:
Centralized Metadata Management
Standards + metadata maintained in a global repository for greater consistency and content reuse.
Complete Traceability
Version control, governance workflows, and audit tracking provide complete traceability and accountability of metadata
Faster Study Setup
Automate study spec generation from master standards for higher quality, more efficient setup.
Integrated Validation and Real-Time Collaboration
In-stream validation and real-time chat means errors are identified and resolved early in the process, avoiding delays at the end.
Why you shouldn’t miss this chance to see what Pinnacle 21 Enterprise can do for your business
💪 See how to grow in ways you can’t with Excel or standalone tools
💪 Learn how automation can de-risk your processes
💪 See the impact this kind of technology can have on submission timelines
Book a demo today
Schedule a demo or consultation to see how Pinnacle 21 can accelerate your path from study design to submission.
Driving results for leading pharma organizations
"Pinnacle 21’s MDR is very intuitive and user-friendly, so there is no steep learning curve like you might get with other systems. The integrated validation mechanism means we can do real-time validation, right from the start.”
Radhika Kale
Associate Director of Statistical Programming Standards, Alnylam Pharmaceuticals
