Cobridge is a regulatory affairs consulting firm that provides comprehensive product-registration services for medical products in Japan. We offers a comprehensive list of regulatory services, in formulating best cost-effective regulatory strategies, in preparing application documents, and in communicating with the Ministry of Health, Labor and Welfare (MHLW) and the Pharmaceuticals and Medical Devices Agency (PMDA). Through a wide range of services, including regulatory affairs, clinical studies, Designated Marketing Authorization Holder (DMAH), preparation of drug master files (DMFs) and acting as their In-Country Caretaker (ICC), we supports clients entering the Japanese market with their medical products including pharmaceuticals and medical devices.

Cobridge Co.,Ltd.

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