Become a VERA Alpha Program Member
What Device. What Happened. What Outcome — Finally Connected.
Unleash the power and simplicity of the VERA™ Essentials.
Register. Validate, and track your stock of FDA Class I, II or III medical devices for expiration, near expiration, recalls, and adverse events.
Don’t worry about integrating UDI into your exiting inventory or ERP system.
You receive a private, cloud-based account to track all your medical device inventory, and be ready to track implanted medical device performance in your patients!
Why Become a VERA Alpha Program Member?
Work with Innovators
The challenges in transitioning to UDI in your supply chain and clinical procedure workflows is a complex, daunting challenge. Our VERA platform creates a safe, open, and accessible collection of UDI data for your business and clinical operations.
Full Health Clarity will work directly with you to train you on how to perform key workflows, but we will work to tune the product to better meet your needs.
As a VERA Alpha Program Member, you’ll
Gain Early Access to our fully integrated UDI tracking and analytics platform.
Influence Development by sharing feedback that shapes workflows, reporting, and usability.
Realize Efficiency Gains that reduce costs, improve compliance, and enhance patient safety.
Elevate Your Reputation as a leader in healthcare innovation.
Confirmed VERA Alpha Program Members receive:
The opportunity to evaluate the VERA Essentials System for up to one year. The evaluation includes access to the VERA software service Admin pages and a VERA Mobile Access Kit.- The VERA Mobile Access Kit uses the device camera to register medical devices into the VERA Essentials System. The VERA Mobile Access Kit includes a mobile device and VERA Essentials Software. Additional kits are available to Alpha Program Members only, for the pre-release price of $495 USD.
Dedicated support during business hours will be provided to help you get the most from your evaluation.
Early access to new features, with priority given to ideas you suggest!- Recognition in Full Health Clarity case studies, presentations, and industry publications (optional)
Proven Impact You Can Expect
From early pilot data and industry benchmarks, hospitals implementing FHC’s UDI Platform have seen:
50%-95%
reduction in labor costs to identify and notify patients about recalled devices
More than 95%
reduction in risk of medical errors from expired or recalled products
5-10%
reduction in on-hand inventory
10-30%
reduction in labor costs to manage inventory
50-100%
reduction in expired item costs
Less than 1%
rate of device selection errors
How It Works
1. Integration
We connect with your existing ERP, EHR, and inventory systems.
3. Analytics
Real-time insights and longitudinal data improve decision-making.
2. Automation
Automated recall, adverse event, and expiration tracking begins.
4. Outcome Tracking
Link devices to patient outcomes for proactive surveillance and risk reduction.
What We Ask from VERA Alpha Program Members
Assign a project lead for implementation and coordination
Participate in regular feedback and review sessions
Allow anonymized data sharing to validate performance metrics
Commit to a defined preview release period (typically 6–12 months)
Be Part of the Movement
Every year, U.S. hospitals face billions in costs from medical device recalls, inventory waste, and litigation risk. Together, we can change that.
Join us in building a healthcare system where every device decision is informed by real-world data – delivering safer procedures, smarter choices, and better patient outcomes, everywhere.