Japan should fundamentally overhaul its cost-effectiveness assessment (CEA) scheme while putting a hold on CEA-based price adjustments, a new ruling…
REGULATORY
PMDA Strengthens Consultation System to Support Biomarker Development
In response to advances in drug development and personalized medicine using genomic pharmacology, the Pharmaceuticals and Medical Devices Agency (PMDA) has strengthened since April 1 its consultation system with respect to pharmacogenomics (PGx) and biomarkers (BMs). In addition to establishing…
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REGULATORY
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