Huma receives multi-condition US FDA 510(k) Class II regulatory clearance for its configurable SaMD disease management platform
Class II clearance expands the patient population that can be managed Companies working with Huma’s platform can now launch algorithm innovations more quickly in a compliant and de-risked manner, democratising digital health innovation across the industry Clearance was granted through the FDA’s joint eSTAR programme which aims to increase the efficiency of regulation through digitalisation NEW YORK … Read more