CRF Health is First to Gain FDA Registration, and 21CFR 820 Recognition, of their TrialMax® ePRO System as Medical Device

PLYMOUTH MEETING, Pa.--(BUSINESS WIRE)--In accordance with the new FDA regulation, set in April this year, CRF Health’s TrialMax® has become the first ePRO system to complete its Medical Device registration, a regulation that concerns medical device data systems (MDDS) that collect information from apparatus such as spirometers and glucometers.