REGULATORY
PMDA Testing New System that Uses Electronic Medical Information to Help Assess Post-Marketing Drug Risk
The Pharmaceuticals and Medical Devices Agency (PMDA) has started a “MIHARI (Medical Information for Risk Assessment Initiative) Project” to test new post-marketing safety measures. The project is testing a new system for secondary use of electronic medical information such as…
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In the complex landscape of the Japanese pharmaceutical market, the “status quo” is often the safest harbor. But for leaders like Kennet Brysting, former president of Gilead Japan, the status quo is the most dangerous place to stay.Innovation in Japan…





