Healthcare Software Built to Perform
DataArt helps healthcare and life sciences organizations build and modernize platforms, scale AI capabilities, and improve clinical workflows, without compromising compliance or patient safety.
![DMT 12639 [Gartner Mention] BANNER](https://websitesapi.dataart.com/media/bnwhcomj/dmt-12639-gartner-mention-banner.webp)
Built for Healthcare Growth
Digital Health Consulting
We build compliant digital health software, from strategy to delivery, with regulatory expertise and AI workflows that shorten your time to market.
Learn More
Scale Your HIS Infrastructure
We design, integrate, and scale HIS infrastructure with compliance, interoperability, and AI-enabled workflows built in for long-term performance.
Learn MoreGoverned by Design
Healthcare software delivery demands more than engineering capability. It demands accountability, auditability, and confidence that every system you build operates within your compliance framework.
Regulatory adherence across HIPAA, GDPR, ISO 13485, ISO 27001, EU MDR/IVDR, US FDA, NIST, EHDS, and other applicable local regulations
- Implementations run in your environment — your data, your IP, your control
- Audit-ready workflows and documentation across the full software lifecycle
- Artisyn's governed delivery model embeds compliance checkpoints by design, not as a final review stage
This approach was recognized in the 2025 Everest Group’s “Healthcare Data, Analytics, and AI Services PEAK Matrix® Assessment,” which recognized DataArt as a Major Contender.
Trusted by Healthcare Leaders
Transforming Patient Experience: Helping Patients Manage Surgeries at Northwell Health's Petrocelli Surgical Pavilion
From Pharmaceutical to Digital Health: A Strategic Leap Through SaMD Development
Industry Recognitions
A Smarter Way to Build Enterprise Software
Strategic Partners
Industry Insights
Health Data as a Strategic Asset: Interoperability, AI, and EHDS Readiness as Competitive Advantage for Digital Health
Validating AI in Software as a Medical Device (SaMD): Meeting MDR, GDPR, and EU AI Act Requirements
From Regulation to Implementation: Translating the EU AI Act into Product Requirements for Medical Devices
AI in Medical Devices: Lifecycle Integration and Regulatory Readiness
From Data to Trust: Validating AI in Medical Devices with Real-World Data
From Data to Trust – Validating AI in Medical Devices with Real-World Data
New FDA Requirements for Connected Medical Devices: How Cybersecurity Impacts Regulatory Approval
New FDA Requirements for Connected Medical Devices
Healthcare AI Regulations in EU, UK, and US: Comparative Analysis
AI-Enhanced Digital Health: How AI Can Make a Difference for Personalized Therapy
The Role of AI in Clinical Trials: Insights from Industry Experts
ClinicAI: Transforming Clinical Trials
FDA Compliance Challenges in Medical Device Software Engineering
AI in Clinical Trials: Increase Speed and Efficiency while Cutting Cost and Error Rates
Three Pillars of Clinical Development in Precision Medicine: Complex Data, AI/ML, Regulatory Compliance
Your Roadmap to DiGA Excellence: Seven Tips for Product Managers
Data Analytics in DiGA and Digital Therapy
HIPAA Compliance with AWS Policy as Code: A Code-Driven Approach to Healthcare Security
Optimizing NCBI Data Synchronization: Effective Approaches and Key AWS Services
The Digital Revolution: Reimagining Healthcare Through Technology and a Whole Health Approach
Our Team
Whether you're building or scaling a health information system, bringing a healthcare software product to market, or embedding governed AI into clinical workflows, DataArt's healthcare team is ready to move.
Share your details, and we'll be in touch within 24 hours.
