Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Invites Opinions on Candidate Drugs for JP Listing
The Pharmaceuticals and Medical Devices Agency (PMDA) on October 5 began inviting opinions on new drug candidates for listing in the Japanese Pharmacopoeia (JP). Opinions will be accepted until November 7. The new drug candidates are: losartan potassium-hydrochlorothiazide tablets, telmisartan,…
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REGULATORY
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