Crouch j d (52 Ergebnisse)

Paperback. Zustand: As New. No Jacket. Pages are clean and are not marred by notes or folds of any kind. ~ ThriftBooks: Read More, Spend Less.

Zustand: 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.

Zustand: Good. Good condition. A copy that has been read but remains intact. May contain markings such as bookplates, stamps, limited notes and highlighting, or a few light stains. NOT AVAILABLE FOR SHIPMENT OUTSIDE OF THE UNITED STATES.

Hardcover. Zustand: As New. No Jacket. Pages are clean and are not marred by notes or folds of any kind. ~ ThriftBooks: Read More, Spend Less.

Hardcover. Zustand: As New. No Jacket. Pages are clean and are not marred by notes or folds of any kind. ~ ThriftBooks: Read More, Spend Less.

Soft cover. Zustand: Very Good. ORIGINAL 1978 PUBLICATION; ex-corporate library; in very good condition. Book.

Soft cover. Zustand: Very Good. ORIGINAL 1978 PUBLICATION; ex-library; light creasing of corners of wraps and leaves; o/w in very good condition. Book.

Zustand: Good. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.

Zustand: Very Good. Very Good condition. Reprint No. 1418 from the Public Health Reports Vol. 45, No. 41, October 10, 1930 (Pages 2429-2432). Minor edge-chipping.VG for the booklet's age. (infectious disease vaccine innoculation).

Paperback. Zustand: Very Good. All investigators funded by the National Institutes of Health are now required to receive training about the ethics of clinical research. Based on a course taught by the editors at NIH, Ethical and Regulatory Aspects of Clinical Research is the first book designed to help investigators meet this new requirement. The book begins with the history of human subjects research and guidelines instituted since World War II. It then covers various stages and components of the clinical trial process: designing the trial, recruiting participants, ensuring informed consent, studying special populations, and conducting international research. Concluding chapters address conflicts of interest, scientific misconduct, and challenges to the IRB system. The appendix provides sample informed consent forms. This book will be used in undergraduate courses on research ethics and in schools of medicine and public health by students who are or will be carrying out clinical research. Professionals in need of such training and bioethicists also will be interested.…

Paperback. Zustand: Fair. Reprint. The item might be beaten up but readable. May contain markings or highlighting, as well as stains, bent corners, or any other major defect, but the text is not obscured in any way.

Zustand: Good. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.

Paperback. Zustand: Good. The Oxford Textbook of Clinical Research Ethics is the first comprehensive and systematic reference on clinical research ethics. Under the editorship of experts from the U.S. National Institutes of Health of the United States, the book's 73 chapters offer a wide-ranging and systematic examination of all aspects of research with human beings.Considering the historical triumphs of research as well as its tragedies, the textbook provides a framework for analyzing the ethical aspects of research studies with human beings. Through both conceptual analysis and systematic reviews of empirical data, the contributors examine issues ranging from scientific validity, fair subject selection, risk benefit ratio, independent review, and informed consent to focused consideration of international research ethics, conflicts of interests, and other aspects of responsible conduct of research.The editors of The Oxford Textbook of Clinical Research Ethics offer a work that critically assesses and advances scholarship in the field of human subjects research. Comprehensive in scope and depth, this book will be a crucial resource for researchers in the medical sciences, as well as teachers and students.…

Paperback. Zustand: New. For over forty years professor Harold W. Rood developed provocative theories in strategy, international relations, diplomacy and military power, and American foreign policy. Rood's teaching and corpus of original writing greatly influenced generations of students who would go on to play key leadership roles in government and the public policy community. This book synthesizes Rood's core teachings to preserve them for future generations and to stimulate new thinking in his intellectual legacy.…

Zustand: new.

Zustand: New. Professionals in need of such training and bioethicists will be interested. Editor(s): Emanuel, Ezekiel J.; Crouch, Robert A.; Arras, John D.; Moreno, Jonathan D. Num Pages: 528 pages, 2, 2 black & white line drawings. BIC Classification: MBDC. Category: (G) General (US: Trade); (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly. Dimension: 279 x 217 x 33. Weight in Grams: 1516. . 2003. 1st Edition. Paperback. . . . . …

PAP. Zustand: New. New Book. Shipped from UK. Established seller since 2000.

PAP. Zustand: New. New Book. Shipped from UK. Established seller since 2000.

Zustand: New. 2017. paperback. . . . . .

Paperback. Zustand: New. All investigators funded by the National Institutes of Health are now required to receive training about the ethics of clinical research. Based on a course taught by the editors at NIH, Ethical and Regulatory Aspects of Clinical Research is the first book designed to help investigators meet this new requirement. The book begins with the history of human subjects research and guidelines instituted since World War II. It then covers various stages and components of the clinical trial process: designing the trial, recruiting participants, ensuring informed consent, studying special populations, and conducting international research. Concluding chapters address conflicts of interest, scientific misconduct, and challenges to the IRB system. The appendix provides sample informed consent forms. This book will be used in undergraduate courses on research ethics and in schools of medicine and public health by students who are or will be carrying out clinical research. Professionals in need of such training and bioethicists also will be interested.…

Zustand: New.

Zustand: New. pp. 530 12:B&W 8.5 x 11 in or 280 x 216 mm Perfect Bound on White w/Gloss Lam.

paperback. Zustand: Very Good. Cover and edges may have some wear.

Zustand: As New. Unread book in perfect condition.

Paperback. Zustand: Brand New. 257 pages. 9.00x6.00x0.75 inches. In Stock.

Zustand: New. In English.

Zustand: New. 2017. paperback. . . . . . Books ship from the US and Ireland.

Zustand: New. Professionals in need of such training and bioethicists will be interested. Editor(s): Emanuel, Ezekiel J.; Crouch, Robert A.; Arras, John D.; Moreno, Jonathan D. Num Pages: 528 pages, 2, 2 black & white line drawings. BIC Classification: MBDC. Category: (G) General (US: Trade); (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly. Dimension: 279 x 217 x 33. Weight in Grams: 1516. . 2003. 1st Edition. Paperback. . . . . Books ship from the US and Ireland. …

Hardcover. Zustand: Brand New. 224 pages. 11.00x9.00x0.91 inches. In Stock.

Zustand: Good. This is an ex-library book and may have the usual library/used-book markings inside.This book has soft covers. Clean from markings. In good all round condition. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,2100grams, ISBN:9780199768639. …