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Conducting GCP-compliant clinical research / / Wendy Bohaychuk and Graham Ball [[electronic resource]]



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Autore: Bohaychuk Wendy Visualizza persona
Titolo: Conducting GCP-compliant clinical research / / Wendy Bohaychuk and Graham Ball [[electronic resource]] Visualizza cluster
Pubblicazione: Chichester ; ; New York, : John Wiley, c1999
Descrizione fisica: 1 online resource (xiv, 211 p. )
Disciplina: 615/.1901
Soggetto topico: Clinical trials - Standards
Drugs - Testing - Standards
Onderzoek
Geneeskunde
Clinical Trials as Topic - standards
Drug Evaluation - standards
Drug Evaluation, Preclinical
Evaluation Studies as Topic
Drug Discovery
Investigative Techniques
Epidemiologic Methods
Health Care Evaluation Mechanisms
Quality of Health Care
Public Health
Environment and Public Health
Health Care Quality, Access, and Evaluation
Health Care
Clinical Trials as Topic
Drug Evaluation
Medicine
Health & Biological Sciences
Medical Research
Soggetto genere / forma: Computer network resources.
Electronic books.
Altri autori: BallGraham  
Note generali: Bibliographic Level Mode of Issuance: Monograph
Nota di bibliografia: Includes bibliographical references (p. 202-205) and index.
Sommario/riassunto: Conducting GCP-Compliant Clinical Research Wendy Bohaychuk and Graham Ball Good Clinical Research Practices, UK and Canada The overall aim of this work is to provide a reference book which describes the general framework for conducting GCP-compliant clinical research, particularly pharmaceutical industry clinical research. Wendy Bohaychuk and Graham Ball run a consultancy, GCRP Ltd., which has conducted over 820 GCP audits involving more than 200 companies in the last 10 years. More than 5,000 individuals have been involved in their training courses to help people perform GCP-compliant clinical research. They have authored several books and articles including: Standard operating procedures for investigators Standard operating procedures for sponsors and CROs GCP - an indexed reference Drawing on their wealth of experience, they have produced this enlightening and practical reference work which fills an educational gap in the understanding of GCP at all levels.; Written in concise language simple enough to be accessible to those new in the field, the dozens of real-life stories and detailed case studies at the end of each chapter make the book an invaluable resource for the more experienced, highlighting what can go wrong in a clinical study: A study of prostate cancer in the UK - An investigator brochure was not provided. The company argued that a brochure was unnecessary because the drug was already marketed. Indeed it was - for hypertension! A study of cardiovascular surgery in the UK - The consent dates were changed (by overwriting) to indicate that the patients had provided consent before the study started. The original dates post-dated the start of the study. A study of hypertension in Germany - The investigator brochure predated the study by nine years! Checklists are provided throughout the book to help monitors, auditors and investigators
ensure that nothing important is overlooked.; The authors present the topic of GCP with remarkable clarity, insight and enthusiasm emphasizing that this code of practice was not designed to make studies more difficult for investigators or more expensive for sponsors and CROs but, in the final analysis, to ensure the safety and well-being of study participants and future patients who will benefit from well-conducted, GCP-compliant studies.
Titolo autorizzato: Conducting GCP-compliant clinical research  Visualizza cluster
ISBN: 1-280-55482-7
9786610554829
0-470-32599-2
0-470-84626-7
Formato: Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione: Inglese
Record Nr.: 9910830553503321
Lo trovi qui: Univ. Federico II
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