Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
JPMA Official Calls for Partial Introduction of CDISC-Based Electronic Applications; Runup Period too Short
Masaaki Kuwahara (Senior Director, Regulatory Affairs Department, Development Center Japan, Pharmaceutical Development Division, Takeda Pharmaceutical), chairman of the Japan Pharmaceutical Manufacturers Association’s (JPMA) Regulatory Affairs Committee, spoke on the electronic applications that will become mandatory from FY2016 at a symposium…
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