Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA to Launch “GMP Roundtable” with Academia, Industry
The Pharmaceuticals and Medical Devices Agency (PMDA) said on March 22 that it will set up a “GMP roundtable” to bring together relevant representatives from companies, regulatory authorities, and academic institutions to share challenges in the arena and discuss solutions.…
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