Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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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