Benefits of generative AI software development in healthcare
Why implement AI in healthcare with NEKLO
20+
years in business
300+
launches in regulated sectors
150+
healthcare development experts
5.0
Clutch rating
85%
of clients stay with us long term
7%
turnover rate — stable, senior teams
Why to develop AI medical software with NEKLO
Secure delivery
Accountability
Transparency
Predictable delivery
Cultural fit
Compliance by design
Our AI healthcare software development services
AI medical imaging
Reduce diagnostic delays and errors with explainable imaging AI clinicians can trust. Enhanced by clinician override and safety guardrails, our AI medical image analysis tools designed for FDA/CE pathways with explainability and audit trails to ease regulatory review.

Clinical NLP and documentation automation
Cut hours of clinical documentation and coding time. NEKLO builds HIPAA-ready NLP models that can be integrated with major EHRs (Epic, Cerner, Allscripts), as well as FHIR APIs. We create solutions for clinician adoption, solving burnout and interoperability issues.

AI predictive analytics in healthcare
Get real-time, interoperable models with validated MLOps for risk management and operational forecasting. Our solutions cover readmissions, staffing needs, no-shows, and resource bottlenecks. Predictions stay accurate, explainable, and audit-ready, addressing tech debt, failed dashboards, and poor ROI visibility.

Virtual health assistants
Boost patient satisfaction with AI medical assistants that provide safe, accurate guidance. We build secure, compliant, clinician-supervised AI assistants, minimizing risks like diagnostic errors and unsafe outputs. Our chatbots increase patient satisfaction and provide tailored guidance.

AI in hospital revenue cycle
We deliver healthcare AI software for revenue cycle automation that accelerates charge capture, coding, and claims. Our solutions reduce manual effort, lower denials, and speed up reimbursements — fully aligned with ICD-10, CPT, HL7, and HIPAA/CMS rules.

Remote patient monitoring
NEKLO builds software under IEC 62304/ISO 13485 standards, making connected medical devices reliable in real clinical use. Our solutions process data, filter false or irrelevant signals, and reduce alert fatigue, integrating with wearables and monitoring systems for safe, trusted care.

Artificial intelligence in pharmacology
We provide regulatory-ready data infrastructure with validation and full traceability. Designed for pharmacology and life sciences research, our AI powered healthcare solutions support safety audits, streamline clinical trial data handling, and speed regulatory acceptance.

Generative AI for medical knowledge management
Our experts design and train domain-adapted GenAI with bias safeguards and human-in-the-loop controls. Built for compliance-sensitive use cases, it enables safe knowledge management, clinical decision support, and operational automation — addressing black-box risks and liability fears.




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Technologies
Languages and frameworks
Model Ops and automation
NLP and generative AI
Computer vision
Case studies
Our collaboration models
FAQ
Can you work with limited or messy data?
Of course. We start generative AI healthcare applications with a feasibility assessment, clarify ground truth, and design around data gaps. Our team uses transfer learning, synthetic data, or weak labeling to prove value quickly. In addition, we can add targeted data collection (when needed), so projects stay lean and achievable.
How do you handle PHI?
We embed security-by-design principles into every project by default, including strict data minimization, end-to-end encryption, access control, and audit logs to name a few. Our process aligns with HIPAA, GDPR, and SOC 2 standards, ensuring regulatory compliance and client-specific security policies are fully respected.
Will clinicians trust the outputs?
Sure. AI-powered medical apps adoption is a tracked KPI. We design outputs that are interpretable, with clear confidence thresholds and clinician override controls. Human-in-the-loop review is built in. When implementing AI medical software, we involve clinical staff early, running usability tests to ensure tools reduce workload, build trust, and improve daily practice.
What’s a typical first project?
Most clients start AI development with a focused, high-value pilot. Examples include an AI triage flag or automated coding assist. Delivered in 6–10 weeks, pilots integrate with existing workflows, show measurable ROI, and provide a clear path for scaling into broader clinical or operational use cases.
Can AI be validated for regulatory approval?
Yes, we support clients in FDA and CE submissions by preparing validation datasets, detailed traceability documentation, and comprehensive risk analyses. Our team works alongside regulatory consultants to ensure your medical AI software is audit-ready, fully documented, and aligned with IEC 62304 and ISO 13485 standards — reducing delays and increasing the likelihood of approval.
How fast can we move from prototype to production?
Healthcare artificial intelligence software development speed depends on data readiness and regulatory scope. Most clients move from prototype to production-ready MVP in 3–6 months. We deliver quick pilot projects, followed by validation and hardened MLOps, so you can demonstrate value early while building for long-term compliance.