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Updated: Sep 8, 2025

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COVID-19 パンデミックからのEUの学びに基づく,欧州の製薬規制と市場アクセス慣行の将来性:複数の利害関係者インタビューからの洞察

Zilke Claessens1, Grace Beirne2, Catherine Decouttere2

  • 1Clinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium. zilke.claessens@kuleuven.be.

Therapeutic innovation & regulatory science
|September 6, 2025
PubMed
まとめ

ステークホルダーは,迅速なCOVID-19薬の承認が有益であると認めましたが,リソース上の課題も指摘しました. 推奨事項は,将来の健康緊急事態と日常的な枠組みの改善された協力と透明性に焦点を当てています.

キーワード:
コロナウイルス共同調達市場へのアクセスパンデミック対策患者のアクセス定性的な研究規制の枠組み

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