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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We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…





