Japan's medical device market is one of the most robust markets in Asia, but its regulatory system can be confusing. Before deciding to sell your device in the Japanese market, it is important to understand how the regulations apply to your device, which steps to take, and what resources are required to complete the process. In this recorded presentation, Ann Marie Boullie, Vice President of Business Development for EMERGO, discusses some of the most complex aspects of the Japanese registration process, including:
Recorded October 2016
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