The qtec group: A team of experts

As daunting the MDR may seem to many Medical Device manufacturers, our steadily growing team is specialized in easing this fear, and providing a guide though Medical Device Regulation (MDR). As a competent partner, we are able to start at any point in the life cycle of Medical Devices to provide advice and assistance. This cycle begins with Clinical Evaluations, Risk Management, Requirement Engineering, Approval, Verification & Validation, Software Quality and ends with Post-Market Surveillance.

Supporting your company's needs in the most efficient way, and providing you with an expert that fits you and your company's needs is our top priority.