Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Considering Review Procedure Policy for IVD Agents Based on FDA Guidance Draft
Regarding ongoing requirements to enhance the review system for in vitro diagnostic (IVD) agents aimed at promoting personalized healthcare, Pharmaceuticals and Medical Devices Agency (PMDA) Deputy Review Director Daisei Miyamoto (Office of Medical Devices II) revealed at a lecture held…
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