第２２回 医療機器・体外診断薬の承認審査や安全対策等に関する定期意見交換会 議事録 ｜厚生労働省
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第２２回 医療機器・体外診断薬の承認審査や安全対策等に関する定期意見交換会 議事録 ｜厚生労働省
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This page contains the meeting minutes of the 22nd Regular Opinion Exchange Meeting on Medical Device and In Vitro Diagnostic Approval Review and Safety Measures, held on October 7, 2024. Hosted by the MHLW Pharmaceutical Affairs Bureau, the meeting was conducted in hybrid format at PMDA headquarters. The bureau chief discussed the Pharmaceutical Affairs Law revision and the 2024 Collaborative Plan for Optimization of Medical Device Regulation and Review. The ministry emphasized promoting the rapid practical implementation of innovative medical devices utilizing AI technology through strengthened industry cooperation and regulatory optimization.
