Search results for: an-impartial-witness

An Impartial Witness

Author : Charles Todd
File Size : 90.73 MB
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“Todd’s novels are known for compelling plotting with a thoughtful whodunit aspect, rich characterization, evocative prose, and haunting atmosphere.” —Richmond Times-Dispatch “Readers who can’t get enough of [Jacqueline Winspear’s] Maisie Dobbs…are bound to be caught up in the adventures of Bess Crawford.” —New York Times Book Review To great critical acclaim, author Charles Todd introduced protagonist Bess Crawford in A Duty to the Dead. The dedicated World War I nurse returns in An Impartial Witness, and finds herself in grave peril when a moral obligation makes her the inadvertent target of a killer. As hauntingly evocative as Todd’s award-winning, New York Times bestselling Ian Rutledge novels, An Impartial Witness transports readers to a dark time of war and involves us in murder, intrigue, and the fascinating affairs of a truly unforgettable cast of characters.

Institutional Review Board

Author : Elizabeth A. Bankert
File Size : 54.48 MB
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This book is designed as an instructional manual that gives Institutional Review Board (IRB) members and administrators the information they need to run an efficient and effective system of protecting human research subjects, in compliance with federal research regulations. This reference provides a step-by-step approach to practical details of IRB administration and includes case studies, sample forms, and sample policy documents, as well as decision-making algorithms and lists of approval criteria for their resolution.

Informed Consent in Medical Practice Principles and Convention

Author : D Kalidas Chavan
File Size : 71.24 MB
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An Overview of Clinical Trial Operation

Author : Shibadas Biswal
File Size : 54.75 MB
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This book is a must-read for students and professionals for a broad understanding of the entire process of clinical trial operation. In the second edition released in December 2017, we have added several new topics of interest taking the total count to 112. At the moment, a clinical trial is the most relevant method at our disposal to explore and establish safety/efficacy of a new medicine. It is the fundamental basis of clinical development programs of healthcare products. Clinical research has opened up several new career choices. Graduates in medicine, pharmacy, and other life sciences now have the option to work as investigators, scientists, project managers, data managers, monitors, study coordinators, regulatory affairs managers, and so on. Many of these positions have specialized and focused responsibilities in the industry setting. Considering the highly complex environment of clinical research, a broad overview is indispensable for effective collaboration. This book has been written for life science graduates aspiring to work in clinical research industry or clinical research professionals without considerable experience in trial operation. It would also be useful for professionals with focused responsibilities to broaden understanding of the entire gamut of trial operation. As fundamental approach is independent of nature of the investigational product (e.g. drug, device, vaccine or diagnostic agent), we are hopeful of its wider usefulness to the entire healthcare industry. The objective is to provide a broad outline of key activities, principles, roles, and responsibilities without getting into procedural details. Most organizations involved in clinical research have defined processes and procedures to carry out specific responsibilities relevant to their business. Hence, the discussion is purposefully limited to an overview to keep it concise yet informative. Discussion in each topic covers the background, operational overview, and usual challenges. Frequently used terminology has been introduced in the context of specific topics to induce familiarity. The book has been organized into several topics from the perspective of a project manager driving an entire trial. Organization of topics is according to the flow of trial operation from conception to the end. At the outset, the context of different trials according to phases of drug development has been introduced. Subsequent topics are on planning, setup, execution, and closeout in a sequential manner. Towards the end, the topics are on few general aspects of trial operation. This book has been written based on our practical experience, as well as regulatory guidance and other freely accessible literature. Good clinical practice (GCP) lays down the fundamental guiding principles for trial operation. Familiarity with any GCP guidance is highly recommended for the best outcome from this book.

Christ all and in all A series of discourses

Author : George ROBSON (of Lauder.)
File Size : 53.26 MB
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100 Questions and Answers About Research Ethics

Author : Emily E. Anderson
File Size : 67.22 MB
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100 Questions (and Answers) About Research Ethics by Emily E Anderson and Amy Corneli is an essential guide for graduate students and researchers in the social and behavioral sciences. It identifies ethical issues that individuals must consider when planning research studies as well as provides guidance on how to address ethical issues that might arise during research implementation. Questions such as assessing risks, to protecting privacy and vulnerable populations, obtaining informed consent, using technology including social media, negotiating the IRB process, and handling data ethically are covered. Acting as a resource for students developing their thesis and dissertation proposals and for junior faculty designing research, this book reflects the latest U.S. federal research regulations to take effect mostly in January 2018.

Theodore Tilton Vs Henry Ward Beecher

Author : Theodore Tilton
File Size : 82.95 MB
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Nazareth Against Nice Or An Impartial View of the Existing Churches Their Creeds and Principles from the Stand point of the Written Word of God

Author : Henry Hardy
File Size : 78.32 MB
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Courts of Exchequer and Exchequer Chamber

Author : William Newland Welsby
File Size : 22.8 MB
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A Very Young Couple

Author : Fanny Wheeler Hart
File Size : 56.35 MB
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Plain Truth

Author : Eye witness
File Size : 30.53 MB
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The Nova Scotia reports

Author :
File Size : 28.5 MB
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The Nova Scotia Reports

Author : Nova Scotia. Supreme Court
File Size : 36.84 MB
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Plain truth or An impartial account of the proceedings at Paris during the last nine months By an eye witness

Author : Plain truth
File Size : 33.36 MB
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Journal of the House of Representatives of the State of Michigan

Author : Michigan. Legislature. House of Representatives
File Size : 54.37 MB
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Includes extra sessions.

Law of distress completed laws of hostage sureties fosterage saerstock tenure daer stock tenure and of social connections

Author :
File Size : 62.75 MB
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Hiberniae Leges Et Institutiones Antiquae

Author :
File Size : 89.54 MB
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Injuries of the Spine and Spinal Cord Without Apparent Mechanical Lesion and Nervous Shock

Author : Herbert William Page
File Size : 53.76 MB
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Reports of cases

Author :
File Size : 49.85 MB
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Reports of Cases Determined in the Appeal and Chancery Divisions and Selected Cases in the King s Bench and at Chambers of the Supreme Court of New Brunswick

Author : New Brunswick. Supreme Court
File Size : 25.2 MB
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