Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Drug Makers Can Now Access MID-NET from Their Own Offices
The Pharmaceuticals and Medical Devices Agency (PMDA) began on July 8 a new service that enables drug makers to use its MID-NET database from their own offices for the purpose of post-marketing surveillance (PMS). The agency hopes that the move…
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REGULATORY
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