Convert fragmented health and product data into interoperable, standards-aligned FHIR outputs—ready for compliance and integration.
Clinical data utility breaks when interoperability relies on rigid point-to-point interfaces and manual mapping. Automated harmonization is required to meet regulatory mandates and fuel real-world evidence (RWE) initiatives.
Patient data is locked in incompatible formats (HL7 V2, C-CDA, PDF, CSV) across disparate EHRs. Aggregating longitudinal records for analysis is technically prohibitive.
Standardizing local codes to global standards (SNOMED, LOINC, RxNorm) requires expensive manual curation. Inconsistencies render data unusable for population health or research.
CMS and ONC mandates demand FHIR readiness. Legacy systems cannot natively expose data via FHIR APIs, creating compliance risks.
Valuable clinical insights exist in free-text notes. Traditional converters drop this unstructured data, creating gaps in the patient narrative.
Bridging the semantic gap with intelligent transformation that converts raw clinical streams into compliant, research-ready FHIR resources.
Deploy intelligent agents to autonomously ingest and map diverse clinical datasets to the FHIR R4 standard. The system parses structural messages (HL7 V2) and unstructured documents (PDFs) simultaneously, identifying resources like Patient, Encounter, and Observation and mapping them to the correct FHIR profiles without manual scripting.
Ensure data fidelity through automated validation workflows that test every resource against specific implementation guides (e.g., US Core, Carin Blue Button). The platform handles exceptions by flagging mapping errors or terminology gaps for steward review. Beyond conversion, the solution delivers intelligence by enriching data with standard ontologies (converting local drug codes to RxNorm), ensuring true semantic interoperability for downstream analytics.
Transition from fragile interfaces to a robust FHIR infrastructure. Achieve the interoperability required to drive digital health innovation and compliance instantly.
reduction in mapping effort
compliance with CMS interoperability rules
faster data onboarding for clinical trials
loss of clinical context
See how raw clinical and regulatory data becomes structured, FHIR-aligned intelligence—ready for integration, analytics, or regulatory exchange.
Automatically convert incoming data streams from varying EHR vendors into a single, canonical FHIR format.
Map local, messy codes to standard ontologies like LOINC and SNOMED automatically to ensure analytical validity.
Aggregate disparate patient records into longitudinal files instantly to support clinical trial matching and evidence generation.
Expose clean, validated FHIR APIs to authorized third-party apps and partners with granular consent management.




Find clarity on our solutions, capabilities, and how we can support your business.
Botminds allows for extensive customization, enabling users to set specific keywords, department filters, and other criteria. This flexibility ensures that the FHIR compliance process aligns perfectly with your organizational goals.
Our platform is built to scale, efficiently managing high volumes of compliance records from multiple sources. Advanced algorithms and machine learning models adapt to various document formats and data types, ensuring consistent processing quality.
Botminds offers comprehensive support, including detailed documentation, training sessions, and dedicated customer service. We ensure that your team is well-equipped to use the platform effectively and maximize its benefits.
Absolutely! Botminds is designed to process various formats, including electronic documents, printed materials, and handwritten notes. Our flexible extraction models can seamlessly handle diverse data sources.
Book a 30-minute consultation to find the best starting point