Stocked with knowledge on Global Medical Devices Regulatory Affairs, we are well equipped to assist in development and commercialization of Medical Devices hailing from nascent stages (TRL 1-3) to advanced stages (TRL 7-9).
Extensive Regulatory experience of development and commercialization of more than 500 Medical Devices (implantable, non-implantable, in-vitro diagnostic devices) ranging across varied Risk Classifications.
Paired with adequate expertise on Development of Medical Devices and Quality with engineering and regulatory aspects, the combination is guaranteed to be a formidable asset for all your Medical Device regulatory requirements.