[{"data":1,"prerenderedAt":24},["ShallowReactive",2],{"$f-D8SMtdWlzdvSIFvkrBkFU8pVNGffHvqAwIorLIv8fQ":3},{"card":4,"examId":6,"chapterTitle":22,"prev":15,"next":23},{"id":5,"examId":6,"prompt":7,"answer":8,"choices":9,"questionType":12,"explanation":13,"explanationDetail":14,"mistakeHint":15,"lectureRef":15,"storyRef":15,"chapterSlug":16,"sectionCode":17,"sectionTitle":18,"clusterSlug":19,"term":15,"sequenceOrder":20,"regionWeight":15,"revisionMark":15,"isActive":21},"ch4-001","touhan","薬機法の目的は、医薬品等の品質・有効性・安全性の確保と保健衛生の危害防止に加え、研究開発の促進により保健衛生の向上を図ることである。",0,[10,11],"正しい","誤り","ox","薬機法第1条に定められた目的です。規制・指定薬物対策・研究開発促進を通じて保健衛生の向上を図ることが目的とされています。","薬機法第1条の目的は三本柱で構成されています。①品質・有効性・安全性の確保と危害防止規制、②指定薬物の規制措置、③特に必要性が高い医薬品・医療機器・再生医療等製品の研究開発促進、の3つです。",null,"chapter-4","4-I","薬機法の目的等","yakuhou-mokuteki",1,true,"第4章 薬事関係法規・制度","ch4-002",1784619074317]