Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Plans to Increase Inspection Staff in Response to Kaketsuken Scandal
The Pharmaceuticals and Medical Devices Agency (PMDA) will increase the number of its inspectors in response to the scandal over GMP violations by the Chemo-Sero-Therapeutic Research Institute (Kaketsuken), a PMDA official said on December 16. Tomiko Tawaragi, PMDA chief safety…
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REGULATORY
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