QAdvis AB is based in Sweden with two offices – Lund and Stockholm. We are about 25 senior and expert consultants supporting clients worldwide, with an emphasis on Scandinavian and European companies. We are a longtime trusted service provider for the medical device and in vitro diagnostic device industry.
We offer a complete range of multidisciplinary services within quality, regulatory and clinical evidence. This include European Authorized Representation services for non-EU manufacturers and UK Responsible Person services for non-UK based manufacturers from our British office QAdvis UK Ltd.
Our team members are very experienced and active participants in several key international standardization committees and EU commission workgroups, writing standards and guidelines. We do this work to find the most cost effective approach to your regulatory challenges.
Over the years, our team has successfully conducted a large number of expert assignments, thereby establishing partnerships and alliances with clients, industry, trade associations and an international network of expert consultants.