Medical Device Registration in Japan
GRP Medical Device Services in Japan:
Global Regulatory Partners Inc, (GRP) affiliate in Japan, (Global Regulatory Partners GK) located in Tokyo has a local team of regulatory affairs professional who can help you register your medical device with PMDA.
Global Regulatory Partners GK is registered with PMDA as Marketing Authorization Holder (category 1), can act as you MAH or DMAH in Japan and handle all your regulatory affairs, clinical, quality and pharmacovigilance needs in Japan.
Check out this video to get a better understanding about our services in Japan for medical devices.