Medical Device Software
Development & Consulting
We provide consulting expertise and contracting services for
- Quality Management & Regulatory Affairs
- Cybersecurity, Cloud Solutions and Risk Management
- Automation and Digitalisation in MedTech
- Medical Software Development
- Project Management
Medical Device Regulatory Affairs Consulting
Practical and tailored compliance for your business

ISO 13485
Quality Management System
We set up your Quality Management System to benefit your company—simple, automated, and digitized.
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IEC 62304
Medical Device Software
Your developers will get confidence that they focus only on things that matter and leave superfluous work behind.
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ISO 14971
Medical Device Risk Management
Let's make your Risk Management clear and practical, building your team’s confidence in every step while ensuring patient safety.
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IEC 81001-5-1
Cybersecurity of Health Software
We take the complexity out of cybersecurity compliance, ensuring your software is secure through clear, practical, and understandable solutions.
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ISO/IEC 27001
Information Security and Privacy Protection
We implement a security framework that protects your business and patient data while being easy to understand, efficient, and fully tailored to your needs.
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NIS2
Cybersecurity Directive
Even complex EU cybersecurity requirements become manageable with us—we’ll guide you through NIS2 compliance in a practical, stress-free way.
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EU MDR
Medical Device Regulation
We handle the complexity of EU MDR for you, ensuring compliance with clear, streamlined processes that fit seamlessly into your business.
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FDA 21
Quality System Regulation
We’ll help you meet FDA requirements effortlessly, creating a quality system that works for you and ensures smooth product approvals.
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EU AI Act
Quality System Regulation
We guide you through the EU AI Act, ensuring your AI-powered medical devices comply with clear, practical, and ethical requirements.
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Medical Software Development & Project Management
Put your software in trusted hands!
- Development of Medical Device Software with complete Technical Documentation including Risk Management File ready for regulatory submission
- Expertise in IEC 62304, ISO 14971, and FDA 21 CFR 820.30, validated by MDR and FDA audits
- Integration of MDR, GDPR, and cybersecurity for compliance and secure audit outcomes
Why To Work With Us
Driven by responsibility, backed by experience
- Successfully built multiple QMS systems achieving ISO and CE certifications
- Working with key players in the global pharmaceutical and medical device market
- A strong track record in healthcare and software solutions

Nice To Meet You
Hi, I'm Vaclav, a medical doctor with over 15 years of experience in the world of software.
I've assisted various companies in building their Quality Management Systems from the ground up and obtaining CE Certification for their Medical Device Software.
I have collaborated on medical device development with renowned companies such as:
- Novartis
- Roche
- Merck
- Ypsomed
Together with my team, consultants and developers, we help companies succeed in the medical device industry.
What They Said About Us
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