Abmed Medical Technology
Your trusted partner for seamless medical device regulatory registration,
offering expert representation in the EU and UK markets
Your Authorized Representation for Europe
Seamless Market Access
We provide expert regulatory representation to help non-EU products enter the EU and United Kingdom markets with ease.
Regulatory Compliance
Non-EU manufacturers are required by local regulations to appoint an authorized representative for EU market access. We ensure full compliance by acting as your local contact for competent authorities.
Strategic Location
With offices in Ireland and the UK, we offer fast communication channels and an in-depth understanding of local regulations, enabling smooth and efficient product registration.
Fast and Safe Market Entry
Our expertise ensures that your product reaches the market quickly and safely, minimizing delays and maximizing compliance.
Since our establishment in 2008, we have become a leading global provider of medical device regulatory registration services.
Over the past 10 years, we have proudly served more than 1,000 healthcare clients and over 100 publicly listed companies.
Our commitment to excellence and customer satisfaction has been the cornerstone of our success, allowing us to consistently deliver top-quality services and solutions to our clients.
OUR
STORY
Comprised of a number of R&D, technical and quality professionals with senior backgrounds in the pharmaceutical industry and senior consultants,
we are a consulting firm specialising in multinational medical regulatory registration services.