[{"data":1,"prerenderedAt":27},["ShallowReactive",2],{"$fAEnr2ll7qk4Z4xbpuGQ3wiJU4gO6L4MkIT9gz1aU3ks":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},"ch1-024","touhan","製造販売後の調査・試験の実施基準はどれか。",2,[10,11,12,13],"GCP","GVP","GPSP","GLP","four","製造販売後の調査や試験の基準は「GPSP」です。Post-marketing（市販後の）Study（調査・試験）という英単語が由来です。","同じ製造販売後の段階でも、GVPは「安全管理（Vigilance）」の基準を指します。「調査」か「管理」かで区別しましょう。","「GPSP（調査・試験）」と「GVP（安全管理）」の意味を逆に回答させる引っかけがよく出ます。",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","ch1-023","ch1-025",1784619073794]