We are global provider for verifying the compliance of medical devices at every stage of their life cycle.
From initial design and development through manufacturing, distribution, and post-market surveillance, we ensure that medical devices meet all regulatory and safety standards, providing comprehensive and reliable validation services.
Global Expertise
With several laboratories and offices strategically located around the world, we maintain a strong international presence.
This global distribution enables us to stay at the forefront of technical advancements, ensuring an up-to-date knowledge of international regulatory scenarios, shared across our network.
Specialization
Our team consists of highly skilled professionals in the medical sector (medical devices, in vitro diagnostic medical devices and combination products) who undergo continuous, specialized training to stay ahead in medical devices field, working in technologically advanced laboratories.
Unique Reference
Thanks to the strong integration and synergy between the companies of the group and our highly qualified network, we act as a unique reference service provider for the verification of Medical Devices compliance, testing and verifying all phases of the medical device life cycle and thus satisfy every customer request.
Strategic Regulatory Medical Devices Consulting Worldwide
We are committed to saving the lives and preserving the health of humankind by demonstrating the compliance throughout the whole life-cycle of the medical devices.
For this reason, we provide our Clients with full set of services which enable them to market increasingly safe and effective quality products in the national and international markets.
Working at the Highest Certification Standards
We work to obtain and maintain the necessary certifications to attest the conformity of our facilities, companies and laboratories in an act of respect and protection for our customers.
