[{"data":1,"prerenderedAt":27},["ShallowReactive",2],{"$fM5ohXOvvqLPSZt0ZOYyYdGj8Fmy4jhWcKv_xQ5XySio":3},{"card":4,"examId":6,"chapterTitle":24,"prev":25,"next":26},{"id":5,"examId":6,"prompt":7,"answer":8,"choices":9,"questionType":14,"explanation":15,"explanationDetail":16,"mistakeHint":17,"lectureRef":18,"storyRef":18,"chapterSlug":19,"sectionCode":20,"sectionTitle":21,"clusterSlug":22,"term":18,"sequenceOrder":18,"regionWeight":18,"revisionMark":18,"isActive":23},"ch1-019","touhan","医薬品の非臨床試験（動物実験等）の実施基準として正しいものはどれか。",2,[10,11,12,13],"GCP（Good Clinical Practice）","GPSP（Good Post-marketing Study Practice）","GLP（Good Laboratory Practice）","GVP（Good Vigilance Practice）","four","正解は「GLP（Good Laboratory Practice）」です。これは動物などを使った「非臨床試験」の実施基準を指します。","その他の基準も頻出です。\n・GCP：ヒトを対象とする「臨床試験」の基準\n・GPSP：市販後の「調査・試験」の基準\n・GVP：市販後の「安全管理」の基準\nそれぞれの違いを整理しておきましょう。","「GLP」と「GCP」など、似たようなアルファベットの略語を入れ替える問題はよく狙われます。",null,"chapter-1","1-I-2","医薬品のリスク評価","risk-hyouka",true,"第1章 医薬品に共通する特性と基本的な知識","ch1-018","ch1-020",1784619073788]