Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Nearly 60% of Face-to-Face Consultations from July 2011 through September 2013 Involved Drugs: PMDA
Yasunori Yoshida, director of the Pharmaceuticals and Medical Devices Agency’s (PMDA) Office of Review Management, reported the results of the PMDA’s regulatory strategy consultation services over the past two years at a forum on pharmaceutical affairs strategy on November 19.…
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REGULATORY
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