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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

ISO 13485

Quality Management System

IEC 62304

IEC 62304

Medical Device Software

ISO 14971

ISO 14971

Medical Device Risk Management

IEC 81001-5-1

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

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

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

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

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

EU AI Act

Quality System Regulation

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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
ProfileImage

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

Michael Maretzke

CTO

Temedica

Vaclav did support our journey to become ISO 13485 certified with relentless work put into great processes, great communication and detailed and to the point conversations with the teams, individual members - but also our external auditors. He was of great support to move our QMS to the next level. He was the key person behind the move away from paper / scan based documents towards a digital setup.

If you are in need for a structured person with great communication skills, a good understanding of the regulatory environment, I can only recommend to reach out to Vaclav. Lucky you if he's not booked ;-) Besides all the success he's an enjoyable and humble character. Great experience to having worked with him.

Dilli Ramannagari

Risk Manager | Cybersecurity

Ypsomed

Vaclav and I worked together on risk management activities of medical device development projects. His ability to quickly grasp the challenges and to accomplish a task/project is remarkable. Additionally, his ability to propose and develop software solutions to improve projects’ efficiency is commendable. I find Vaclav to be flexible, dependable, and quality centric. Hence, I really enjoyed working with Vaclav and looking forward to associate with him again.

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