Japan’s Ministry of Health, Labor and Welfare (MHLW) on March 5 unveiled the revised NHI prices for drugs subject to…
BUSINESS
Streamline Regulatory Approval Process with Overseas Data: Rakuten Chief
The Pharmaceuticals and Medical Devices Agency (PMDA) should streamline its regulatory approval process by accepting overseas clinical trial data, rather than requiring Japanese data, Rakuten Medical Japan Chairman Hiroshi Mikitani said on October 1. Mr Mikitani made the call as…
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