Services
Engineering high-quality
software for healthcare
We help healthcare and medical device companies build certification-ready custom medical software. Our end-to-end software services for medical devices combine regulatory requirements with Agile methodologies. Compliance is built into the development process while keeping projects on a controlled timeline and budget.
Industries
Our services for medical devices
Not sure which services fit your project?
We’ll shape the right services to your individual needs.
About Revolve Healthcare
Who we work with
We collaborate with teams responsible for building and maintaining regulated healthcare products, including:
Medical Device Manufacturers,
MedTech Startups,
Pharma,
Hospitals and Clinics,
BioTech,
Mental Health,
Animal Health
Our role in a medical device project
(Revolve Healthcare)
Product responsibility
You are responsible for the product as a whole and for bringing it to the market
We focus on digital part of the project – delivering safe and reliable software
Regulatory compliance
You coordinate the overall regulatory and compliance process
We support you with documentation and evidence of compliance within the software scope
Documentation
You combine all required documentation of your medical device into one consistent set
We prepare technical software documentation that can be easily integrated to yours
Design & development
You define the business goals and intended use of the product
We support your process and design, develop, and maintain the software within the scope you choose
Testing & cybersecurity
You make final decisions regarding product-level testing and risks
We perform software-level testing and safety analysis within our scope
Post-market support
You manage the product after market launch
We provide technical maintenance, updates, and data to support ongoing product management
Timeline
How does our collaboration start?
Discovery meeting
we review your product concept, regulatory context, and technical scope.
Project Proposal
we prepare a scope, timeline, and delivery model aligned with your product roadmap.
Agreement
we formalise our cooperation and establish the legal and confidentiality framework.
Kickoff
a dedicated team of specialists integrates with your workflow and development environment.
Schedule a free strategic consultation.
In this 45-minute session, we can:
review your software concept,
clarify MDR or IVDR requirements,
outline a realistic development path,
answer technical or regulatory questions.
This meeting is non-binding and focused on giving you clarity before making any decisions.
Launch Faster, Without Compliance Headaches
Bringing medical software to market? Avoid costly delays.