Textbook of Clinical Trials
Sold by BOOKWEST, Phoenix, AZ, U.S.A.
AbeBooks Seller since December 10, 2022
New - Hardcover
Condition: New
Ships within U.S.A.
Quantity: 1 available
Add to basketSold by BOOKWEST, Phoenix, AZ, U.S.A.
AbeBooks Seller since December 10, 2022
Condition: New
Quantity: 1 available
Add to basketUS SELLER SHIPS FAST FROM USA. NEW: TEXTBOOK OF CLINICAL TRIALS 2004 HARDCOVER Textbook of Clinical Trials by David Machin (Editor), Simon Day (Editor), Sylvan Green (Editor), Brian S. Everitt (Editor), Stephen George (Editor) OUR REFERENCE: 127E3-129E4-131F-.0471987875-HC-2Pt4-D13 DESCRIPTION A comprehensive volume on clinical trials that covers all important disease and therapeutic areas together with methodologies, phase I/II/III studies and other issues. The volume catalogues the impact of clinical trials on the practice of medicine and discusses the developments and practice of medical statistics. Cancer, cardiovascular disease, dermatological, dental, mental, ophthalmic health, gynaecology and respiratory diseases are all discussed in separate chapters, with discussions on outcome measures, competing risks and statistical models given for each therapy area. It also presents: * A history of clinical trials * A summary of pertinent statistical issues * How to choose a clinical trial design * Ethical constraints and considerations * Clinical trial issues in paediatrics and those involving older patients * Clinical trials in complementary medicine Product details Publisher ‏ : ‎ Wiley (March 12, 2004) Language ‏ : ‎ English Hardcover ‏ : ‎ 428 pages ISBN-10 ‏ : ‎ 0471987875 ISBN-13 ‏ : ‎ 978-0471987871.
Seller Inventory # 129E4-131F-0471987875-HC-2Pt4-D13
Uniquely this Textbook addresses issues as they impact on patients with diseases in the following specific areas:
In addition, chapters deal with special issues in children and older patients.
This is an essential reference for all involved with clinical trials. It will be of particular relevance to clinical trialists, whether with administrative, data management and quality, scientific or statistical roles, workers in the pharmaceutical industry, those who sit on ethics committees, work in regulatory departments or grant awarding bodies and doctors taking part in the conduct of clinical trials.
Draws together critical information in one key text
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