Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Says “Slow Cartagena Review” Is Urban Legend, Set to Dispel Misconception
There have been calls from the pharma industry for Japan to ease regulations around the Cartagena Act, contending that the law is delaying time-to-market for gene therapies in the country. But the Pharmaceutical and Medical Devices Agency (PMDA) rebuts this…
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