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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A few weeks ago, I had coffee with a very talented executive. Let’s call him Kenji. He has a great job, a big salary, and a solid team. But he was unhappy. He felt bored and wanted a new challenge.…





