After Product Registration After product registration in Japan, a foreign medical device company&rs

After Product Registration
After product registration in Japan, a foreign medical device company’s products and the classifications of those products will be the basis of the services required for a MAH or DMAH. There are several different fee schedules for ongoing DMAH services. Companies that are willing to pay the fees for an independent third party DMAH, choose to do so in order to have greater control over their product registration, product marketing, and retention of their confidential information.

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Despite a declining population, foreign device companies that are successful in Japan still have significant opportunities to reap large benefits.