In order to perform clinical trials efficiently in Japan : Important issues in medical institutions raised by the GCP on-site review

• AKIYAMA Teppei

  The Office of Conformity Audit, Pharmaceuticals and Medical Devices Agency

• FURUTA Mitsuko

  The Office of Conformity Audit, Pharmaceuticals and Medical Devices Agency

• YAMADA Hiroshi

  The Office of Conformity Audit, Pharmaceuticals and Medical Devices Agency

Bibliographic Information

Other Title

• わが国の治験の円滑化のために(1) : GCP実地調査から見た医療機関での留意点

Journal

• 日本呼吸器学会雑誌 = The journal of the Japanese Respiratory Society

  日本呼吸器学会雑誌 = The journal of the Japanese Respiratory Society 44 (8), 541-549, 2006-08-10

Keywords

• Clinical trial
• GCP
• Clinical investigator
• Sub-investigator
• Human subjects

Details

• CRID: 1570291225436217216
• NII Article ID: 10018813133
• NII Book ID: AA1119595X
• ISSN: 13433490
• Web Site: https://search.jamas.or.jp/link/ui/2006290223
• Text Lang: ja
• Data Source:
  • CiNii Articles