辉瑞gcp培训资料

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课件分类:药学
课件类型:参考资料
文件大小:265.67KB
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课件目录与文件树:
  • 辉瑞gcp培训
    • 辉瑞GCP培训
      • 1-Clinical Research-An Overview中文.doc(25600)
      • 10-Evaluation of a Clinical Research Site(Part 1)中文.doc(23552)
      • 10-Evaluation of a Clinical Research Site(Part 2)中文.doc(22528)
      • 11-The Protocol as a Clinical Research Tool(Part 1)中文.doc(24576)
      • 11-The Protocol as a Clinical Research Tool(Part 2)中文.doc(21504)
      • 12-Trial Documents(Part 1)中文.doc(21504)
      • 12-Trial Documents(Part 2)中文.doc(22016)
      • 13-The Responsibilities of Conducting a Clinical Trial(Part 1)中文.doc(22528)
      • 13-The Responsibilities of Conducting a Clinical Trial(Part 2)中文.doc(23552)
      • 14-Clinical Supplies Management中文.doc(20992)
      • 15-Safety Reporting Responsibilities中文.doc(27136)
      • 16-Guidelines for CRF Completion(Part 1)中文.doc(24064)
      • 16-Guidelines for CRF Completion(Part 2)中文.doc(20992)
      • 17-Trial Monitoring(Part 1)中文.doc(22016)
      • 17-Trial Monitoring(Part 2)中文.doc(20480)
      • 18-Audit of a Clinical Trial Site(Part 1)中文.doc(21504)
      • 18-Audit of a Clinical Trial Site(Part 2)中文.doc(22016)
      • 19-Clinical Research in the 21st Century(Areas for Future Research)(Part 1)中文.doc(20992)
      • 19-Clinical Research in the 21st Century(Areas for Future Research)(Part 2)中文.doc(24064)
      • 19-Clinical Research in the 21st Century(Areas for Future Research)(Part 3)中文.doc(21504)
      • 2-Historical Development of International Regulations in Clinical Research(Part 1)中文.doc(23552)
      • 2-Historical Development of International Regulations in Clinical Research(Part 2)中文.doc(22528)
      • 20-(ICIC) A Model of a Private Health Institution for Clinical Research(Part 1)中文.doc(23552)
      • 20-(ICIC) A Model of a Private Health Institution for Clinical Research(Part 2)中文.doc(24576)
      • 3-Overview of the ICH GCP Guideline中文.doc(24576)
      • 4-The Institutional Review Board and The Ethics Committee(Part 1)中文.doc(24064)
      • 4-The Institutional Review Board and The Ethics Committee(Part 2)中文.doc(23040)
      • 5-Informed Consent(Part 1)中文.doc(20992)
      • 5-Informed Consent(Part 2)中文.doc(19968)
      • 5-Informed Consent(Part 3)中文.doc(21504)
      • 6-Phases of Drug Development(Part 1)中文.doc(23552)
      • 6-Phases of Drug Development(Part 2)中文.doc(26624)
      • 6-Phases of Drug Development(Part 3)中文.doc(23040)
      • 7-Clinical Trial Design(Part 1)中文.doc(26112)
      • 7-Clinical Trial Design(Part 2)中文.doc(25088)
      • 8-Basic Concepts in Applied Statistics(Part 1)中文.doc(23552)
      • 8-Basic Concepts in Applied Statistics(Part 2)中文.doc(22528)
      • 8-Basic Concepts in Applied Statistics(Part 3)中文.doc(25088)
      • 辉瑞GCP培训c.doc(267264)
  • 说明.txt(348)

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