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Managing Humans: Biting and Humorous Tales of a Software Engineering Manager (Paperback)
Michael Lopp
Managing Humans is a selection of the best essays from Michael Lopps web site, Rands In Repose. Drawing on Lopp's management experiences at Apple, Netscape, Symantec, and Borland, this book is full of stories based on companies in the Silicon Valley where people have been known to yell at each other. Whether you're an aspiring manager, a current manager, or just wondering what the heck a manager does all day, there is a story in this book that will speak to you.
Principles and Practice of Clinical Research, Second Edition (Principles & Practice of Clinical Research) (Hardcover)
John I. Gallin (Editor) Frederick P. Ognibene (Editor)
A comprehensive reference that addresses the theoretical and practical issues involved in conducting clinical research.
Clinical Trials: A Practical Approach (Hardcover)
Stuart J. Pocock (Author)
This comprehensive, unified text on the principles and practice of clinical trials presents a detailed account of how to conduct the trials. It describes the design, analysis, and interpretation of clinical trials in a non-technical manner and provides a general perspective on their historical development, current status, and future strategy. Features examples derived from the author's personal experience.
Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary (Paperback)
Ezekiel J. Emanuel (Editor)
Robert A. Crouch (Editor)
John D. Arras (Editor)
Jonathan D. Moreno (Editor)
Christine Grady (Editor)
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.