"Principles and Practice of Clinical Research" is a comprehensive text which addresses the theoretical and practical issues involved in conducting clinical research. This book is divided into three parts: ethical, regulatory, and legal issues; biostatistics and epidemiology; technology transfer, protocol development and funding. It is designed to fill a void in clinical research education and provides the necessary fundamentals for clinical investigators. It should be of particular benefit to all individuals engaged in clinical research, whether as physician or dental investigators, Ph.D. basic scientists, or members of the allied health professions, as well as both students and those actively participating in clinical research. It includes comprehensive review ranging from a historical perspective to the current ethical, legal and social issues and an introduction to biostatistics and epidemiology. It is a practical guide to writing a protocol, getting funding for clinical research, preparing images for publication and display. It is a cohesive and clear presentation by authors carefully selected to teach a very popular course at NIH. It is an excellent companion text for courses on clinical research.
Le informazioni nella sezione "Riassunto" possono far riferimento a edizioni diverse di questo titolo.
"...this book clearly fulfills an important function for anyone involved in clinical research...this book will be accessible to a wide range of readers...this book is much needed and provides essentially all of the basic information required by investigators involved in clinical research, from both a practical perspective and a regulatory perspective...it is an excellent starting point for those embarking on a clinical research project, as well as a valuable reference that experienced investigators will probably want to have readily available."-THE NEW ENGLAND JOURNAL OF MEDICINE (April 2003)
"...a comprehensive treatment of the subject of clinical research...current and timely...an asset to a library or personal collection...Dr. John Gallin, Editor, is also an NIH clinical researcher...he and the majority of the 42 contributors are employed by the NIH...therefore, much of the content of this book is in the public domain, an added plus for instructors and students...subject selectors would be interested in all three of the books...however, the work by Dr. Gallin is the most comprehensive of the three...although corporations and universities conduct their own clinical research, they receive funding from or partner with this government agency...this book is recommended for university and hospital libraries...it can also serve as a textbook for undergraduate and graduate health sciences and science majors...faculty members who engage in clinical research would also benefit from having this volume in their personal collection."-E STREAMS(June 2003)
"This book is much needed and provides essentially all of the basic information required by investigators involved in clinical research. ...an important resource for institional libraries and IRBs."
THE NEW ENGLAND JOURNAL OF MEDICINE
"...this volume provides an outstandingly comprehensive introduction to the field and can be recommended for virtually anyone who is interested in clinical research."
CLINICAL INFECTIOUS DISEASES
"Full of practical advice, top tips and the ever useful "Supplemental Reading" section, it even has a sample face sheet and a study design "tick list"."
IMMUNOLOGY NEWS
"...this book will benefit students, researchers, and clinical practitioners in allied health professions. It is recommended for larger academic and health science libraries."
AMERICAN REFERENCE BOOKS ANNUAL
"Suitable for use as a supplementary textbook or reference."
BOOK NEWS
Preface.
Acknowledgements.
Historical Perspective and Introduction.
Part I: Ethical, Regulatory and Legal Issues
Ethical Principles in Clinical Research.
Researching a Bioethical Question.
Integrity in Research: Individual and Institutional Responsibility.
Institutional Review Boards.
Data and Safety Monitoring Boards.
Data and Data Management in Clinical Trials.
Unanticipated Risk in Clinical Research.
The Regulation of Drugs and Biological Products by the Food and Drug Administration.
Legal Issues.
NIH Policy on the Inclusion of Women and Minorities as Subjects in Clinical Research.
Part II: Biostatistics and Epidemiology
An Introduction to Biostatistics: Randomization, Hypothesis Testing and Sample Size.
Design and Conduct of Observational Studies and Clinical Trials.
Small Clinical Trials.
Large Clinical Trials Clinical Research Institutes.
Using Secondary Data in Statistical Analysis.
An Introduction to Survival Analysis.
Measures of Function and Health Related to Quality of Life.
Economic Analysis and Clinical Research.
Part III: Technology Transfer, Protocol Development and Funding
Overview of Technology Development.
Technology Transfer.
Telemedicine Systems.
Animal Models of Human Disease.
Conducting and Evaluating Clinical Research on Complementary and Alternative Medicine.
Preparing Scientific Images for Publication and Display.
Writing a Clinical Protocol The Mechanics.
Navigating the Peer Review Process for Grants.
Le informazioni nella sezione "Su questo libro" possono far riferimento a edizioni diverse di questo titolo.
Da: Goodwill of Central and Coastal Virginia, Richmond, VA, U.S.A.
Condizione: acceptable. Codice articolo CCVV.0122740653.A
Quantità: 1 disponibili
Da: -OnTimeBooks-, Phoenix, AZ, U.S.A.
Condizione: very_good. Gently read. May have name of previous ownership, or ex-library edition. Binding tight; spine straight and smooth, with no creasing; covers clean and crisp. Minimal signs of handling or shelving. 100% GUARANTEE! Shipped with delivery confirmation, if you're not satisfied with purchase please return item! Ships USPS Media Mail. Codice articolo OTV.0122740653.VG
Quantità: 1 disponibili
Da: HPB-Red, Dallas, TX, U.S.A.
hardcover. Condizione: Good. Connecting readers with great books since 1972! Used textbooks may not include companion materials such as access codes, etc. May have some wear or writing/highlighting. We ship orders daily and Customer Service is our top priority! Codice articolo S_467420105
Quantità: 1 disponibili
Da: ThriftBooks-Atlanta, AUSTELL, GA, U.S.A.
Hardcover. Condizione: Very Good. No Jacket. May have limited writing in cover pages. Pages are unmarked. ~ ThriftBooks: Read More, Spend Less. Codice articolo G0122740653I4N00
Quantità: 1 disponibili
Da: ThriftBooks-Dallas, Dallas, TX, U.S.A.
Hardcover. Condizione: Good. No Jacket. Pages can have notes/highlighting. Spine may show signs of wear. ~ ThriftBooks: Read More, Spend Less. Codice articolo G0122740653I3N00
Quantità: 1 disponibili
Da: Virginia Martin, aka bookwitch, Concord, CA, U.S.A.
Hardcover. Condizione: Fine. Quarto, hardcover, fine, as new, in blue pictorial boards. unmarked. 493 pp. a comprehensive text which addresses the theoretical and practical issues involved in conducting clinical research.divided into three parts: ethical, regulatory, and legal issues; biostatistics and epidemiology; technology transfer, protocol development and funding. It is designed to fill a void in clinical research education and provides the necessary fundamentals for clinical investigators. It should be. Book. Codice articolo 79786
Quantità: 1 disponibili
Da: Wonder Book, Frederick, MD, U.S.A.
Condizione: Fair. Acceptable condition. A readable, intact copy that may have noticeable tears and wear to the spine. All pages of text are present, but they may include extensive notes and highlighting or be heavily stained. Includes reading copy only books. NOT AVAILABLE FOR SHIPMENT OUTSIDE OF THE UNITED STATES. Codice articolo K10OS-00366
Quantità: 1 disponibili
Da: Wonder Book, Frederick, MD, U.S.A.
Condizione: Very Good. Very Good condition. A copy that may have a few cosmetic defects. May also contain light spine creasing or a few markings such as an owner's name, short gifter's inscription or light stamp. NOT AVAILABLE FOR SHIPMENT OUTSIDE OF THE UNITED STATES. Codice articolo L12B-02560
Quantità: 1 disponibili