Medical device interoperability
Connect with hospitals, clinical systems, and future healthcare data networks through secure, standards-based medical device interoperability designed for adoption, scalability, and regulatory readiness.
Why do medical device companies work with us?
MedTech companies work with us when market success depends on medical device interoperability, seamless connectivity with healthcare systems and the ability to exchange data across clinical ecosystems.
We design interoperable medical software that supports integration with existing healthcare infrastructures, helping reduce implementation barriers, especially for hospitals and clinics. This enables medical device manufacturers to collaborate more effectively with healthcare providers, implementing their solutions into existing workflows.
Common interoperability challenges in MedTech
Difficult integration with varied healthcare ecosystems
Limited access to external clinical data
Lack of interoperability-by-design
Uncertainty due to evolving regulatory requirements
High cost and complexity of redesigns
Difficulties scaling product across markets
How do we build interoperability into medical software?
Seamless integration with healthcare systems
Interoperable and scalable platforms
Readiness for future interoperability regulations
HL7 FHIR expertise embedded into delivery experts on board
Seamless integration with healthcare systems
Enable your medical software to connect with the healthcare ecosystem your clients already use, without disrupting workflows or increasing integration time or costs. Make your solution patient-centric and easy for healthcare professionals to use.
We design and implement connectivity with key clinical systems, including Hospital Information Systems (HIS), Laboratory Information Management Systems (LIMS), and Electronic Health Records (EHR), improving software interoperability and ensuring smooth data flow across clinical environments.
Interoperable and scalable platforms
Build a foundation that allows healthcare data to be shared and used across multiple stakeholders in your country.
We develop platform architectures that support controlled data exchange, making your solution a trusted source of clinical data. When integrating your platform with an external system, we use the newe
Readiness for future interoperability regulations
Stay ahead of evolving European interoperability requirements and build a medical device interoperability strategy to reduce the risk of costly redesigns or delays when bringing your product to market.
We continuously monitor initiatives such as the European Health Data Space (EHDS) and evolving national frameworks (e.g. DiGA interoperability in Germany). Our team supports clients in aligning their solutions with emerging regulatory and technical expectations, including implementing HL7 FHIR-based interoperability interfaces when required.
HL7 FHIR expertise embedded into delivery experts on board
Reduce integration risks, improve data sharing reliability, and ensure your solutions align with internationally recognised standards through work with interoperability specialists.
As Revolve Healthcare, we are a member of HL7 International, helping clients develop software interfaces that conform to HL7 FHIR standards. Our team combines certified FHIR expertise with medical device development experience to enable secure, seamless healthcare connection through the idea of interoperability-by-design.
Discuss your interoperability strategy
Schedule a meeting with our experts and discuss your project’s needs and requirements.
What you get working with us
faster and safer implementation with hospital and clinical systems
reduced integration risks through alignment with HL7 FHIR
solution ready for scalable data exchange in the future
clear guidance on architecture and standards
How do we work with you?
We serve as your critical medical software supplier within your quality and regulatory framework, while you remain the legal manufacturer responsible for the device. This strengthens audit-readiness and reduces compliance risks.
We are interoperability-focused throughout the development process, treating data exchange as a crucial part of the project rather than a separate operation. We adapt our approach to your project’s specific technical and regulatory requirements, including compliance with IEC 62304, ISO 14971, and ISO 27001, while ensuring alignment with secure information flow standards and connectivity to external systems.
Case study
Check out how we work through real-life projects:
About Revolve Healthcare
A healthcare interoperability software partner for connected, audit-ready medical solutions.
We build interoperability into our medical software development process from day one. Operating within an ISO 13485-certified QMS and using our Agile 62304 framework to align our activities with IEC 62304, ISO 27001, ISO 14971, ISO 29119-1, and IEC 62366.
We have contributed to more than ten MDR- and IVDR-aligned software projects, covering end-to-end development and legacy systems refactoring.
Let's talk
Build interoperable, compliant, and reliable medical solutions with expert guidance in data exchange.
During a 45-minute free-call you will:
review your current interoperability approach,
explore key certification-related and technical expectations,
address your questions about interoperability.