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A comprehensive and practical guide to clinical trials / edited by Delva Shamley, Brenda Wright, The Clinical Research Centre at the University of Cape Town, Cape Town, Western Cape Province, South Africa.

Contributor(s): Material type: TextTextPublisher: London, United Kingdom ; San Deigo, CA, United States : Elsevier/AP, Academic Press, an imprint of Elsevier, [2017]Copyright date: ©2017Description: xiv, 196 pages : illustrations ; 23 cmContent type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
ISBN:
  • 9780128047293
  • 0128047291
Subject(s): Genre/Form: DDC classification:
  • 615.5072/4 23
LOC classification:
  • R853.C55 C665 2017
NLM classification:
  • W 20.55.C5
Contents:
Introduction to clinical trials / Brenda Wright -- Clinical trial phases / Brenda Wright -- Setting up of site, site assessment visits, and selection / Brenda Wright -- Regulatory requirements / Inge Vermeulen -- Contracts and agreements / Brenda Wright -- Protocol, informed consent documents, and investigator brochure / Brenda Wright -- Planning / Brenda Wright -- Recruitment and retention / Brenda Wright -- Training / Brenda Wright -- Data management / Annemie Stewart -- Investigational medicinal product (IMP) management / Wynand Smythe and Nicky Kramer -- Collecting, processing, and shipment of blood and urine samples / Brenda Wright -- Source document / Brenda Wright -- Screening, treatment, and safety follow-up visit / Brenda Wright -- Quality management / Brenda Wright -- Monitoring, close-out visits, and archiving / Brenda Wright -- Audits and inspections / Brenda Wright.
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Holdings
Item type Current library Collection Call number Status Date due Barcode
Books Books Nepal Health Research Council Book Cart Reference W 20.55.C5/SHA/2017 (Browse shelf(Opens below)) Staff Collection 002280

Includes bibliographical references and index.

Introduction to clinical trials / Brenda Wright -- Clinical trial phases / Brenda Wright -- Setting up of site, site assessment visits, and selection / Brenda Wright -- Regulatory requirements / Inge Vermeulen -- Contracts and agreements / Brenda Wright -- Protocol, informed consent documents, and investigator brochure / Brenda Wright -- Planning / Brenda Wright -- Recruitment and retention / Brenda Wright -- Training / Brenda Wright -- Data management / Annemie Stewart -- Investigational medicinal product (IMP) management / Wynand Smythe and Nicky Kramer -- Collecting, processing, and shipment of blood and urine samples / Brenda Wright -- Source document / Brenda Wright -- Screening, treatment, and safety follow-up visit / Brenda Wright -- Quality management / Brenda Wright -- Monitoring, close-out visits, and archiving / Brenda Wright -- Audits and inspections / Brenda Wright.

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