Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
JPMA Official Hails MHLW Discussions on Use of “Specified Clinical Research” Data in Application Dossiers
A senior official of the Japan Pharmaceutical Manufacturers Association (JPMA) on September 7 welcomed news that the health ministry has started discussions on ways to harness data from so-called “specified clinical research (tokutei rinsho kenkyu)” for drug application dossiers. “We…
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