Data and AI Solutions for Healthcare and Life Sciences

We design every solution around the privacy and security rules that apply to you, such as HIPAA in the United States and GDPR in Europe. That includes encryption in transit and at rest, role-based access aligned with minimum necessary use, audit logging, de-identification where full identifiers are not needed and environments hosted in your cloud tenancy. We also work within your security review and risk assessment processes.

Yes. We implement the FHIR-based APIs and workflows that interoperability rules require, such as Patient Access, Provider Access, Payer-to-Payer exchange and Prior Authorization APIs, using HL7 Da Vinci implementation guides where applicable. We also help with the underlying data mapping, identity management and testing. Because requirements and deadlines differ by organization type and program, we start by confirming your specific obligations with your compliance team.

We integrate with major EHR platforms through their FHIR APIs, HL7 v2 interfaces, vendor app marketplaces and reporting databases, depending on what the vendor and your licenses support. We prefer standards-based integration so solutions remain portable. For workflow tools, we can embed applications inside the EHR using SMART on FHIR or CDS Hooks so clinicians do not need to switch systems.

Safety depends on the use case and the design. We generally start with administrative and documentation tasks where a human reviews every output, such as summarizing records or drafting letters. We ground answers in your own approved content, build evaluation sets with clinicians, log every interaction and define clear boundaries for what the tool must not do. Tools that may qualify as medical device software require additional regulatory assessment, which we flag early.

A focused integration or analytics use case typically reaches production in three to six months. Building an enterprise clinical and claims data platform is usually phased over several releases, with the first data domains available within a few months. Timelines depend mainly on access to source systems, vendor cooperation and internal review processes. We plan these dependencies early and provide weekly written updates so delays are visible.

Yes. For digital health companies we build FHIR-enabled products, data pipelines and AI features with privacy built in. For life sciences organizations we standardize real-world data, build research environments and support analytics for medical affairs and commercial teams. Our pharmaceutical industry page describes our work on GxP-regulated manufacturing and quality data in more detail.