Medical device software maintenance for the post-market phase
We keep your medical software secure, reliable, and compliant while supporting your post-market surveillance activities.

Why do medical device companies work with us?
Medical device software maintenance requires continuous care to keep products secure, reliable, and aligned with ongoing regulatory expectations. As a critical supplier, we help MedTech companies maintain their software through security updates, performance optimisation, and the implementation of changes driven by post-market surveillance (PMS).

Common medical device software maintenance challenges in MedTech
Your software becomes less secure over time
PMS generates more work than your team can absorb
Security vulnerabilities require continuous attention
Every software change must remain compliant
Performances issues start affecting user experience
Cloud infrastructure needs constant monitoring
CAPA actions compete with roadmap priorities
Technical debt slows down product evolution
Software doesn’t keep up with technological advancements
Keeping documentation up to date becomes a burden

Our PMS & maintenance services
Continuous software improvement
Supporting PMS & CAPA activities
Managing security through product’s lifecycle
Infrastructure monitoring & cloud operations
Enhancements and content updates
SLA-based software maintenance
Plan your post-market software maintenance
Schedule a meeting with our experts and discuss your project’s needs and requirements.
What you get working with us
Predictable maintenance costs
Fast incident response
Continuous security improvements
Support for ongoing MDR obligations
Regular maintenance reporting
Service Level Agreement (SLA) tailored to your needs

How do we work with you?
We act as your critical medical software supplier within your quality and regulatory framework, while you remain the legal manufacturer responsible for the device. Our medical device software maintenance services contribute to post-market surveillance, assisting software evolution while maintaining regulatory alignment.
All services are delivered as part of ongoing medical device lifecycle support, while adapting to your project’s specific technical and regulatory requirements, such as compliance with IEC 62304, ISO 14971, and ISO 27001.

About Revolve Healthcare
A maintenance and PMS partner for secure medical software
We help medical software teams keep their systems secure, stable, and compliant throughout the entire product lifecycle. Our maintenance services ensure continuous performance, scalability, and timely updates.
We operate within an ISO 13485-certified QMS and use 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.

Secure the reliability of your software
During a 45-minute free-call you will:
assess your software’s current maintenance demands,
understand regulatory maintenance obligations,
get answers to your questions about our maintenance services