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.
| Other author | Shamley, Delva. |
| Other author | Wright, Brenda. |
| Format | Electronic |
| Publication Info | London, United Kingdom ; San Deigo, CA, United States : Elsevier/AP, Academic Press, an imprint of Elsevier, [2017] |
| Description | xiv, 196 pages : illustrations ; 23 cm |
| Supplemental Content | Full text available from eBook - Pharmacology, Toxicology and Pharmaceutical Science 2017 [EBCPTPS17] |
| Subjects |
| 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. |
| Bibliography note | Includes bibliographical references and index. |
| Access restriction | Available only to authorized users. |
| Technical details | Mode of access: World Wide Web |
| Genre/form | Electronic books. |
| LCCN | 2017936521 |
| ISBN | 9780128047293 |
| ISBN | 0128047291 |
Availability
| Library | Location | Call Number | Status | Item Actions |
|---|---|---|---|---|
| Electronic Resources | Access Content Online | ✔ Available |