REGULATORY
MHLW to Remind Drug Makers of Proper ADR Reporting in Wake of Administrative Improvement Order to Novartis
In the wake of an administrative improvement order issued to Novartis Pharma due to its failure to report adverse drug reactions (ADRs) to its chronic myeloid leukemia treatment Tasigna (nilotinib) within the required period, the Ministry of Health, Labor and…
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REGULATORY
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- Japan Minister Rules Out Full Self-Pay for OTC-Like Drugs
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- Govt’s Bio-WG Wraps Up Biopharma Investment Roadmap Draft
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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…





