Precision. Proficiency. Proximity.
We assist companies with the development and life cycle management of their medical devices, through our global network of regulatory experts, 20+ laboratories, and 2 sterile packaging sites in Europe, North America, & Asia Pacific. Companies of all sizes benefit from our 40+ years of expertise and capabilities to ready their products for market launch and post-marketing activities through three independent services: consulting, testing, and sterile packaging.
Our extensive experience in commercialisation processes, regulatory requirements, and industry trends ensures rapid turnaround of your project with the highest level of service and most advanced technologies.
