M E D I C A L D E V I C E R E G I S T R A T I O N
QH Medical offers full services for the medical device product registration, including clinical trials.
-- Determine product classification;
-- Investigate and evaluate the best route to NMPA (CFDA) approval in China;
-- Development of product registration standards for the NMPA (CFDA) testing;
-- Follow up NMPA (CFDA) testing procedures;
-- Develop clinical protocols, evaluate the hospitals and coordinate clinical trials, if needed;
-- Translate documents and labeling;
-- Prepare final submissions and act as Agent in China (Legal and After Sales), if needed;
-- Follow up with the NMPA (CFDA) after submission;
-- Caretaker for all the registration information and documentation.