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The DI Bulletin provides transparency, insights, strategic updates, and in-depth discussions to clearly communicate our independent trajectory, innovative solutions, and unmatched expertise which defines our leadership in trauma registry technology.
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DI’s ownership group, DI’s leadership team, and DI’s core product & engineering teams have always maintained their independence and were never assimilated into ESO. Moreover, DICORP and its affiliates have always retained rights to:
The DI leadership team, key platform software architects, and an experienced senior team of trauma and registry software experts have remained with DI’s ownership group. None of these personnel were ever transitioned to ESO.
The ownership group also retained ownership of the DI name, domain, and brand.
DI's ownership group made a strategic decision to align with an integration partner to accelerate innovation and expand trauma interoperability. Internal DI decisions made prior to reaching any arrangement ensured:
While DI cannot speak for operations it did not control nor for experiences after 2019, DI’s ownership group followed its 5-year strategic plan:
Now that the planned five-year industry strategy period has ended, DI has reentered the trauma marketplace to ensure its innovations, offerings, and capabilities can be experienced:
From the very beginning, DI’s intent has been to ensure that innovations cost-effectively reach customers who have relied on founder-provided registry solutions since DI’s original founding in 1985 and the release of our first trauma registry solutions in 1987. For 33 years, from 1987 to 2019, DI registry solutions were fully controlled by its founder and ownership group. From 2025 onward, DI ensures that its ownership group retains control to provide constant innovation, exceptional customer service, and unparalleled value for DI customers.
Now, in 2025, we have fulfilled that commitment.
You need only look at the extreme dedication that DI’s founder and ownership group have demonstrated over the past five years to understand our resolve, intent, and commitment to serving this industry. The work trauma professionals perform saves lives and improves outcomes, and for DI, empowering that mission is what drives us every day.
In short, DI retained ownership rights to its core software without restriction and is free to operate without any limitations.
DI's technology excels in this area. Like an iceberg, the majority of the work is within the common core technology. The visible tailoring is just the top layer that adapts to:
DI’s powerful configuration capabilities enable rapid development of industry-specific tailoring that meets compliance and client needs.
DI’s timelines for configuration, onboarding, and go live dates mesh well with trauma centers and health systems compliance cycles and timeline transition objectives.
DI is ready to start projects immediately. Active discussions are already underway with trauma centers and health systems, with timelines aligning well with client objectives.
Why is DI registry customization and implementation so fast?
For more information on DI's 40-year track record, see examples of solutions that are currently in use in the industry, built on DI's original technology, now enhanced by its latest innovations.
Our history of leadership in the trauma registry market includes...
Prior to 2019:
During the past five years, DI has used this time to internally redefine registry technology by:
This technological evolution positions DI as not just a returning leader—but THE driving force in the future of trauma registries.
The DI V7 Platform represents a groundbreaking advancement in trauma registry technology—developed, owned, and operated by DI and its affiliates. Built on modern cloud-native architecture, V7 is the direct continuation of DI’s proven registry solutions, evolved for the next era of performance improvement and healthcare interoperability, while re-establishing DI’s leadership and ground-breaking software innovation.
V7 Trauma Tailoring is being built from the ground up on national NTDS and ITDX standards, supporting ACS TQIP & state/system registry compliance, and reflecting the unmatched expertise of DI’s elite development team.
DI offers customized trauma registry solutions to meet the exacting clinical requirements of trauma centers, health systems, and state and regional trauma registry systems; harmonized with national and state compliance requirements and backed by DI’s unmatched commitment and track record to customer service and support.
DI has also established a Technology Assistance Grant Program to support trauma centers in tailoring their registry solutions for V7 adoption, ensuring smooth transitions and optimal functionality.
A High-Performance, Customizable Approach.
DI’s core philosophy has always been the fusion of robust technology with tailored customization. Our MOTS (modifiable-off-the-shelf) approach allows trauma centers to implement fully compliant registries rapidly—without compromising flexibility or performance. DI has unique and powerful technology to provide this capability. DI has always stood apart in the industry by the extent to which it can customize registry systems, and then support them over the long haul with a track record of decades of exceptional service, reliability, and support. DI is now bringing this track record back into the market for interested centers and trauma systems that want to re-experience the DI Difference made possibly by our unique technology and our leadership-level trauma expertise and focus.
A Fast-Track Approach.
Ensuring rapid deployment while meeting national and state compliance requirements.
Our technology-driven approach cuts traditional customized implementation times dramatically while maintaining full clinical fidelity & regulatory compliance. Our capabilities allow customers to adopt DI solutions quickly and efficiently, ensuring rapid deployment while, at the same time, meeting their individualized and system objectives, harmonized with national and state compliance requirements.
The bottom line: Centers and systems get the exacting clinical specifications they desire for their registries and PI, while ensuring they meet ACS TQIP compliance, and any required state and regional compliance data submission requirements. Moreover, these solutions are built for long term success and backed by a team and technology with a track record to keep its trauma registry solutions well supported and constantly moving ahead.