Shorter time to market with integration of Regulatory Affairs

Our multi-disciplinary team will proactively take steps to deliver innovative medical accessory solutions. We work closely with our customers during prototyping, testing and final production phases and develop your product with Medical Device Regulations in our mind.

Development of a medical accessory requires integration of Regulatory Affairs in every step of the process. To reduce time to market, experience is critical. Our Regulatory Affairs specialists have the expertise to ensure that proper regulatory management is part of your project from the beginning. 

1. Benefit from partnering with Technomed

3. Own manufacturing facilities