Empowering clinical innovation, one trial at a time
We’re on a mission to make clinical trials more accessible, efficient, and impactful.
By providing intuitive eClinical technology, we empower researchers to accelerate medical breakthroughs and improve lives around the world.
Where it began
Our CEO, Stanley Kim, had a clear vision when he wrote the first lines of code behind cubeCDMS – to use technology to address the challenges faced by CROs and sponsors. He wanted to streamline clinical research and simplify the path to data analysis. Today, our development teams remain dedicated to that same goal, continuously advancing our solutions to drive efficiency and innovation.
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The most honorable cause
Many enter the clinical industry by chance – few choose to leave. Like the clients, clinical sites and patients we serve, we are deeply committed to one of the most honorable causes – saving lives and improving the quality of life for those affected by illness. Each day, our clients remind us of the significance of our work, and we are humbled to play our part.
Global vision, local strength
Clinical research thrives when global innovation meets the warmth of local expertise. The vision is simple: to create a future where trials are more human, more flexible, and more connected across borders.
Realizing this vision required a strategic step forward: the acquisition of Mednet on 18th November 2025. This milestone bridges established leadership in Asia with deep operational excellence in North America. CRScube, incorporating Mednet’s 24-year legacy and over 100 FDA-approved clinical trials, brings a unified eClinical platform closer to the people who need it. We are not merely growing in scale; we are expanding our promise to provide expert support right where you are.
Credentials
CDISC ODM certification
FDA 21 CFR Part11 compliance - cubeCDMS v1.1 (incl. IWRS)
FDA 21 CFR Part11 compliance - cubeSAFETY v1.1
CDISC ODM certification
FDA 21 CFR Part11 compliance - cubeCDMS v1.1 (incl. IWRS)
FDA 21 CFR Part11 compliance - cubeSAFETY v1.1
FDA 21 CFR Part11 compliance - cubeCTMS v1.1
FDA 21 CFR Part11 compliance - cubeTMF v1.1
FDA 21 CFR Part11 compliance - cubeCONSENT v1.0
FDA 21 CFR Part11 compliance - cubePRO v1.0
GAMP 5 compliance - cubeCDMS v1.1
GAMP 5 compliance - cubeSAFETY v1.1
EMA compliance - cubeCDMS v1.1
EMA compliance - cubeTMF v1.1
Good software certification - cubeCTMS v1.0
Good software certification - cubeBUILDER v1.0
Good software certification - cubeCDMS v1.0
Good software certification - cubeIWRS v2.0
Good software certification - cubePRO v2.0
Good software certification - cubeSAFETY v2.0
Good software certification - cubeTMF v1.0
ISO 9001:2015
ISO/IEC 27001:2022
WHODrug software certification - cubeCDMS, cubeSAFETY
SCDM industry partner
Our values
Dream with focus
We aim high and dream big, knowing that ambitious goals drive groundbreaking innovation.
Our laser-focused determination turns visionary ideas into reality, propelling the clinical research industry forward.
Create with intent
Like King Sejong, who created Hangul to enrich Korean literacy, we craft solutions with purpose.
Our user-friendly, cost-effective tools democratize clinical research, making it accessible to organizations of all sizes.
Deliver with passion
We pour our hearts into every solution we provide.
Our infectious enthusiasm energizes clients and fuels continuous improvement, helping us persevere through challenges and celebrate shared successes.
Interact with transparency
We build lasting relationships on a foundation of honesty and open communication.
By fostering a culture of transparency, we create an environment of trust that benefits our employees, clients, and the patients we serve.
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