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) specialized 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), MF registration applications, and domestic representative services. Please feel free to contact us for inquiries regarding regulatory submissions for medical devices or master file registrations for active ingredients.