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Cobridge Co., Ltd.

Regulatory affairs consulting for medical devices in Japan.

1999 - Present (26+ years)
Registration

Headquarters: Tokyo, Japan

About Cobridge Co., Ltd.

We are a regulatory affairs consulting firm and supports foreign medical device manufacturers for their medical device registration in Japan.

Why Choose Cobridge Co., Ltd.?

Over 15 years’ experience as a DMAH for medical devices

Staff are scientists with strong technical background and native Japanese + English capability

In-house full-time staff (not virtual firm) for stable long-term client relationships

Comprehensive regulatory services: from gap analysis to post-marketing maintenance

Ability to handle English dossiers and communicate with overseas clients

Cost-effective regulatory strategy for foreign manufacturers

Specializations

4+ Services

Global Presence

1 Offices

Languages

2 Languages

Markets

1 Regions

Recent Updates