REGULATORY
MHLW Study Group to Revise 75 Manuals on Serious ADRs in 19 Fields Over 5-Year Period
A health ministry’s study group began work to revise the “manuals for handling disorders due to adverse drug reactions (ADRs)” at its meeting on October 7. Many members agreed that the manuals need revisions all the way down to their…
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REGULATORY
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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…





