Welcome to Qserve Consultancy B.V.

Qserve Consultancy B.V .
part of the Qserve Group, is an independent medical device regulatory consulting firm operating worldwide, with extensive experience in Europe and the United States. Qserve has considerable in-house expertise in the areas of medical device regulatory affairs, strategic approach, due diligence & GAP analysis, product compliance, training, and quality management systems implementation, and we are familiar with a wide range of devices. Our office is situated in Amsterdam.

Qserve Consultancy
provides coordinated European and American regulatory and quality strategic planning, guidance and implementation from design and development through to market launch, including all regulatory documentation and submissions, to medical device companies around the globe. Our clients include manufacturers of high risk products such as pacemakers, bio-resorbable implants, catheters and combination products. We draw on the excellent relationships we have built up with regulatory authorities, government agencies and testing laboratories, to guide our clients smoothly and swiftly through a large international regulatory network.

Our challenge is to guide and to manage your company in the most efficient and practical ways to achieve registration and market approval.

We respond to meet your needs!

Thank you.