コーブリッジ Company Profile

Professionals will support you in obtaining certification and approval for medical devices.

Our company was founded in 1999 and is a CRO (Contract Research Organization) specializing in regulatory affairs. We support the introduction of medical devices and active pharmaceutical ingredients into the domestic market through a wide range of services, including regulatory submission services, clinical trials, designated marketing authorization holders (DMAH), and master file registration and domestic agent services. Please feel free to contact us for inquiries regarding regulatory submissions for medical devices and master file registrations for active pharmaceutical ingredients.