Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Sets 1st “GMP Roundtable” with Academia, Industry in November
The Pharmaceuticals and Medical Devices Agency (PMDA) said on September 9 that it will hold the first “GMP roundtable” meeting on November 2, bringing together relevant representatives from companies, regulatory authorities, and academic institutions. The PMDA is establishing the confab…
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