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Principles and Practice of Clinical Research -

Principles and Practice of Clinical Research

John I. Gallin (Herausgeber)

Buch | Hardcover
490 Seiten
2002
Academic Press Inc (Verlag)
978-0-12-274065-7 (ISBN)
CHF 125,65 inkl. MwSt
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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 a guide to writing a protocol, getting funding for clinical research,and more.
"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.

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.

Erscheint lt. Verlag 24.1.2002
Zusatzinfo illustrations facsimiles, forms, portraits
Verlagsort San Diego
Sprache englisch
Maße 216 x 279 mm
Gewicht 1371 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete
ISBN-10 0-12-274065-3 / 0122740653
ISBN-13 978-0-12-274065-7 / 9780122740657
Zustand Neuware
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