Developing an innovative medical device is challenging — especially for start-ups navigating complex MDR and FDA requirements with limited resources and tight timelines.
At D.med Technologies, we help MedTech start-ups build compliance from the design stage, turning regulatory complexity into a clear, structured process that supports innovation rather than slowing it down.
From Prototype to Approval — Built on Engineering
Our philosophy is simple: Regulation Built on Engineering.
We integrate regulatory, quality, and cybersecurity principles directly into your development workflow — so compliance becomes part of your device’s DNA.
Our experts combine hands-on engineering experience with regulatory expertise to guide you from initial concept to market approval, ensuring your documentation, testing, and validation meet MDR and FDA expectations.
How We Support Start-ups
✅ MDR & FDA Readiness Assessments – identify compliance gaps and define a realistic roadmap.
✅ Design Documentation & Technical File Setup – align development with Notified Body and FDA requirements.
✅ Cybersecurity & Risk Management Integration – implement IEC 81001-5-1, ISO 14971, and secure-by-design principles early.
✅ Regulatory Strategy Coaching – empower your team to manage compliance efficiently as you grow.
Why Start-ups Choose D.med
Because we understand how medical devices are actually built.
With over 15 years of engineering experience across dialysis systems, digital health platforms, and connected devices, we ensure that compliance and innovation move in sync.
This is how we engineer the path to compliance.
Meet Us at COMPAMED 2025
Join us at Hall 8a / Stand N11 to discuss how we can help your start-up accelerate MDR readiness and bring your innovation to market with confidence.
👉 Book your meeting now: https://calendly.com/dmedtechnologies/30min
Antonios is a Senior Quality & Regulatory Affairs Manager, an accomplished expert in quality management and regulatory compliance regarding development and production of medical devices with over 20 years of experience supporting startups, SMEs and multinational manufacturers.
Antonios specializes in ISO 13485, MDR, and FDA regulations, guiding organizations in the development and implementation of robust quality management systems. Acknowledging Regulatory requirements in a fast paced global environment. His hands-on approach and in-depth knowledge of technical documentation, risk management, software lifecycle management, usability engineering and clinical evaluation ensure that innovations are brought to market efficiently and in full compliance with global standards.
Dedicated to delivering sustainable outcomes, he works closely with partners to enable secure international market access with confidence.