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- catalog contributor b12552723.
- catalog contributor b12552724.
- catalog contributor b12552725.
- catalog created "c2001.".
- catalog date "2001".
- catalog date "c2001.".
- catalog dateCopyrighted "c2001.".
- catalog description "Includes bibliographical references and index.".
- catalog description "The drug development process / John Hall -- Medicinal product regulations in the 21st century / Andrew Willis -- Ethical issues / David Talbot -- Liability and indemnity in clinical research / Angus Donald -- Clinical trial design / Julia Lloyd-Parks -- Early phase studies, pharmacokinetics and adverse drug interactions Phase I studies / Tim Mant -- Phase IV studies / Brian D. Edwards -- The clinical trial protocol / Nina Downes -- Case record form design / Pauline Pentelow -- Clinical trial supplies / Paul O'Connor -- Investigator selection / Shirley Wildey -- Monitoring / John Illingworth -- Drug safety in clinical studies and pharmacovigilance / John C.C. Talbot -- Outcomes research and health economics / Pippa Anderson -- Data management, now and in the future / Karen Grover -- Statistical thinking for clinical trials / Richard Kay -- Project management of drug development / Bryan C. Hurst -- Communicating effectively / Helen Glenny -- Audits and inspections / Pamela Charnley -- Trial master file / Nicola Goodwin -- Archiving / Elizabeth Hooper -- Outsourcing clinical research projects / Wolfgang Schaub -- New directions: regulations for biotechnology products and medical devices / Andrew Willis -- Fraud and misconduct in clinical research / Frank Wells.".
- catalog extent "xvii, 558 p. :".
- catalog identifier "1871816459 (hardcover)".
- catalog issued "2001".
- catalog issued "c2001.".
- catalog language "eng".
- catalog publisher "Petersfield, UK ; Philadelphia : Wrightson Biomedical Pub.,".
- catalog subject "615.1/072/4 21".
- catalog subject "Clinical Trials as Topic".
- catalog subject "Clinical trials.".
- catalog subject "Drugs Testing.".
- catalog subject "QV 771 P9567 2001".
- catalog subject "RM301.27 .P75 2001".
- catalog subject "Research Design.".
- catalog tableOfContents "The drug development process / John Hall -- Medicinal product regulations in the 21st century / Andrew Willis -- Ethical issues / David Talbot -- Liability and indemnity in clinical research / Angus Donald -- Clinical trial design / Julia Lloyd-Parks -- Early phase studies, pharmacokinetics and adverse drug interactions Phase I studies / Tim Mant -- Phase IV studies / Brian D. Edwards -- The clinical trial protocol / Nina Downes -- Case record form design / Pauline Pentelow -- Clinical trial supplies / Paul O'Connor -- Investigator selection / Shirley Wildey -- Monitoring / John Illingworth -- Drug safety in clinical studies and pharmacovigilance / John C.C. Talbot -- Outcomes research and health economics / Pippa Anderson -- Data management, now and in the future / Karen Grover -- Statistical thinking for clinical trials / Richard Kay -- Project management of drug development / Bryan C. Hurst -- Communicating effectively / Helen Glenny -- Audits and inspections / Pamela Charnley -- Trial master file / Nicola Goodwin -- Archiving / Elizabeth Hooper -- Outsourcing clinical research projects / Wolfgang Schaub -- New directions: regulations for biotechnology products and medical devices / Andrew Willis -- Fraud and misconduct in clinical research / Frank Wells.".
- catalog title "Principles of clinical research / edited by Ignazio Di Giovanna, Gareth Hayes.".
- catalog type "text".