Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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Q&A Document on GMP for APIs Reaches Step 4: ICH Meeting in Fukuoka
The Pharmaceutical and Food Safety Bureau’s Evaluation and Licensing Division announced on July 10 the summary results of the meeting of the International Conference on Harmonization (ICH) held last month in Fukuoka. Fifty-five Q&A documents on the Q7 Guideline on…
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