Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
CDISC-Based Electronic Submissions for 24 Products in FY2016: PMDA
Applications for approval using electronic data based on Clinical Data Interchange Standards Consortium (CDISC) formats, which have been accepted since October last year, were filed for 24 products in FY2016 ended March, according to the Pharmaceuticals and Medical Devices Agency…
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REGULATORY
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