소장자료

Quick Guide to Good Clinical Practice How to Meet International Quality Standard in Clinical Research [electronic resource] :

  • Cingi, Cemal. author. , Bayar Muluk, Nuray. author.
  • 2017
Quick Guide to Good Clinical Practice How to Meet International Quality Standard in Clinical Research [electronic resource] :
  • 자료유형
    단행본
  • 서명/저자사항
    Quick Guide to Good Clinical Practice[electronic resource] :How to Meet International Quality Standard in Clinical Research / by Cemal Cingi, Nuray Bayar Muluk.
  • 개인저자
    Cingi, Cemal., author., Bayar Muluk, Nuray., author.
  • 단체저자
    SpringerLink (Online service)
  • 형태사항
    XVIII, 237 p. : online resource.
  • 내용주기
    1 Clinical Trials: Historical Aspects and Importance and New Drug Developments -- 2 The Definition of GCP -- 3 The Principles of GCP -- 4 The Drug Development Process and Evolution of Regulations -- 5 Planning Clinical Research -- 6 Preparation of Ethics Committee (IRB) Proposal -- 7 Preparation of Informed Consent -- 8 Preparation of Findings Tables -- 9 Setting the Ideal Statistical Methods -- 10 The Duties of a Clinical Research Coordinator -- 11 The Duties of Clinical Researchers -- 12 The Phases of Clinical Studies -- 13 Safety in Clinical Trials -- 14 Setting the Size -- 15 Setting the Ideal Method -- 16 Ethics of Clinical Research -- 17 Recruitment and Enrolment -- 18 Why we need Clinical Consent and Other Documentation -- 19 Monitoring the Trial -- 20 Inspection -- 21 Ethics - Institutional Review Board/Independent Ethics Committee(IRB/IEC) -- 22 Responsibilities of the Investigator -- 23 Responsibilities of the Sponsor -- 24.Clinical Trial Protocols.
  • 일반주제명
    Medicine.
    Surgery.
    Pharmacy.
    Medical education.
    Statistics.
    Medicine & Public Health.
    Drug Safety and Pharmacovigilance.
    Statistics for Life Sciences, Medicine, Health Sciences.
    General Surgery.
    Medical Education.
  • 기본자료 저록
    Springer eBooks
  • 기타형태 저록
    Printed edition: 9783319443430
  • ISBN
    9783319443447
  • 언어
    영어