ExpertiseUpdated on 22 January 2026
Regulatory support
About
The qtec Services GmbH is currently a team of almost 100 smart and closely networked experts who see themselves as partners for manufacturers of medical devices. The service we offer, correlates directly with the typical life cycle of a Medical Device. It begins with Requirements Engineering and Risk Management, Software Quality, Verification and Validation, Clinical Evaluation, Registration, and continuing on to Post-Market Surveillance. Our team of experts is happy to support you and your company with the Medical Device Regulation (MDR).
Field
- AI / Predictive Data / Predictive Maintenance
- Medtech /Diagnostics
- Quality Management
- Clinical trials
- Cybersecurity
Similar opportunities
Service
Regulatory and quality management support.
Jochen Harmuth
Director Client Engagement at qtec services GmbH
Lübeck, Germany
Service
Regulatory services for Medical Devices
- E-Health
- Medicine
- Diagnostics
- Medical Devices
- Consulting / Coaching
- Biology/Biotechnology
- Home Care Monitoring Systems
- Hospital/ Rehabilitation Centers
PALOMA LOPEZ-GUERRERO
Consultant in Medical Device Regulation at Episkey Medical Consulting
Madrid, Spain
Service
Medtech Contract Manufacturing
Bernhard Nussbaumer
Managing Director & Co-Owner at ACMIT Gmbh
Wiener Neustadt, Austria