Head Quarters: (+1) 781- 672 - 4200
GRP Japan is located in Tokyo City.
As an PMDA Accredited Market Authorization Holder (MAH) GRP Japan can register Prescription Drugs, OTC, Quasi-drugs, Medical Devices, IVDs and Cosmetics.
Yes, we do.
Yes, GRP Japan quality auditors conduct ISO 13485 and GMP audits for manufacturing sites in Japan Territory.