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独立行政法人 医薬品医療機器総合機構(PMDA)· @PMDA_JPN · X·· 2 小时前精选AI 评分42
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PMDA发布GMP/GCTP年度报告,由其质量管理部编制,该部门负责对日本国内外药品生产场地开展GMP/GCTP检查。报告汇总了检查活动概况、详细检查数据、涉及产业界、政府与学术界的风险沟通工作以及未来规划,并新增专题栏目,涵盖全球协调相关举措。报告全文可在PMDA官网查阅。

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PMDA发布GMP/GCTP年度报告,披露国内外生产场地检查数据与风险沟通做法,可供了解日本检查体系。

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📢【GMP/GCTP Annual Report FY 2025 is now available!】
👉 Full report is here:
https://www.pmda.go.jp/english/review-services/gmp-qms-gctp/0007.html

PMDA has released the “GMP/GCTP Annual Report FY 2024”.
This report from the Quality Management Division, which conducts GMP/GCTP inspections of domestic and overseas pharmaceutical manufacturing sites, provides an overview of our activities, detailed inspection data, risk communication efforts involving industry, government, and academia, and our future vision—all in one volume!
✓ Must-read for the industry
✓ NEW this year: Special Topics!
✓ Includes initiatives on #Globalharmonization

来源:独立行政法人 医薬品医療機器総合機構(PMDA) · x.com