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| View Larger Image | Principles and Practice of Clinical Trial Medicine | Hardcoverby Richard Chin (Author), Bruce Y Lee (Author)
| List Price: | $79.95 | | Price: | $63.96 | | You Save: | $15.99 (20%) | | | Available: | Usually ships in 24 hours |
| | Binding: | Hardcover | | Publisher: | Academic Press | | Edition: | 1st Edition | | Page Count: | 560 Pages | | Publication Date: | July 02, 2008 | | Sales Rank: | 599,140th |
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EDITORIAL REVIEWS | Product Description Clinical trials are an important part of medicine and healthcare today, deciding which treatments we use to treat patients. Anyone involved in healthcare today must know the basics of running and interpreting clinical trial data. Written in an easy-to-understand style by authors who have considerable expertise and experience in both academia and industry, this book covers all of the basics of clinical trials, from legal and ethical issues to statistics, to patient recruitment and reporting results. *Jargon-free writing style enables those with less experience to run their own clinical trials and interpret data.*Book contains an ideal mix of theory and practice so researchers will understand both the rationale and logistics to clinical trial medicine.*Expert authorship whose experience includes running clinical trials in an academic as well as industry settings. *Numerous illustrations reinforce and elucidate key concepts and add to the book's overall pedagogy. |
CUSTOMER REVIEWS (Average Customer Rating: 5.0 based on 1 review)
| A great book by goody 5 Stars April 14, 2009 This is a really well written, comprehensive book. It covers just about anything you'd want to know about clinical studies. It will teach you a lot even if you've been doing clinical research for a while, it's very sophisticated. But not too many equations, although it has a few. You will probably find it very accessible even if you're new to clinical research. Buy it!
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SIMILAR PRODUCTS |

| Clinical Trials - A Practical Guide to Design, Analysis, and Reporting by Duolao Wang (Author), Ameet Bakhai (Author)
Clinical trials form the backbone of evidence-based medicine, and appreciating clinical trial methods allows readers to critique, design and report clinical trials. This book is a friendly 'jargon buster' which aims to demystify the subject. It is divided into five sections: fundamentals of trial design, alternative trial designs, basics of statistical analysis, special trial issues in data analysis, and reporting of trials. Using simple language, the book explains - with ...
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| A Manager's Guide to the Design and Conduct of Clinical Trials (Manager's Guide Series) by Phillip I. Good (Author)
This newly updated edition of the benchmark guide to computer-assisted clinical trials provides a comprehensive primer for prospective managers. It covers every critical issue of the design and conduct of clinical trials, including study design, organization, regulatory agency liaison, data collection and analysis, as well as recruitment, software, monitoring, and reporting. Keeping the same user-friendly format as the original, this Second Edition features new examples and the...
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| FDA Regulatory Affairs: A Guide for Prescription Drugs, Medical Devices, and Biologics, Second Edition by Douglas J. Pisano (Editor), David S. Mantus (Editor)
Examines harmonization of the US Federal Food, Drug, and Cosmetic Act with international regulations as they apply to human drug and device development, research, manufacturing, and marketing. The Second Edition focuses on the new drug approval process, cGMPs, GCPs, quality system compliance, and corresponding documentation requirements. Written in a jargon-free style, it draws information from a wide range of resources. It demystifies the inner workings of the FDA and facilitates an...
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| Fundamentals of Clinical Trials by Lawrence M. Friedman (Author), Curt D. Furberg (Author), David L. DeMets (Author)
This text is intended for the clinical researcher who is interested in designing a clinical trial and developing a protocol. It is also of value to researchers and practitioners who must critically evaluate the literature of published clinical trials and assess the merits of each trial and the implications for the care and treatment of patients. The text uses numerous examples of published clinical trials from a variety of medical disciplines to meaningfully illustrate the fundamentals....
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| Drugs: From Discovery to Approval by Rick Ng (Author)
“Concise and easy to read, the book quickly introduces basic concepts, then moves on to discuss target selection and the drug discovery process for both small and large molecular drugs.” –Doody's Reviews, May 2009 "The second edition of a book that offers a user-friendly step-by-step introduction to all the key processes involved in bringing a drug to the market, including the performance of preclinical trials." –Chemistry World, February 2009 The new edition of...
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