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Principles And Practice Of Clinical Research

Author: John I. Gallin
Publisher: Academic Press
ISBN: 0123821673
Size: 38.64 MB
Format: PDF, Kindle
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This expanded third edition provides an introduction to the conduct of clinical research as well as more comprehensive and expansive content about the infrastructure necessary for a successful clinical research organization or enterprise. With authors who are experts in clinical research in both the public and private sectors, this publication provides essential information to clinical investigators who wish to develop and conduct well designed patient-based research protocols that comply with rigorous study design, ethical, and regulatory requirements.

Principles And Practice Of Clinical Trial Medicine

Author: Richard Chin
Publisher: Elsevier
ISBN: 9780080557939
Size: 74.57 MB
Format: PDF, Docs
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Clinical trials are an important part of medicine and healthcare today, deciding which treatments we use to treat patients. Anyone involved in healthcare today must know the basics of running and interpreting clinical trial data. Written in an easy-to-understand style by authors who have considerable expertise and experience in both academia and industry, Principles and Practice of Clinical Trial Medicine covers all of the basics of clinical trials, from legal and ethical issues to statistics, to patient recruitment and reporting results. Jargon-free writing style enables those with less experience to run their own clinical trials and interpret data Book contains an ideal mix of theory and practice so researchers will understand both the rationale and logistics to clinical trial medicine Expert authorship whose experience includes running clinical trials in an academic as well as industry settings Numerous illustrations reinforce and elucidate key concepts and add to the book's overall pedagogy

Principles And Practice Of Clinical Trial Design

Author: Richard Chin
Publisher: Boston Academic Pub
ISBN: 9780977230228
Size: 57.79 MB
Format: PDF, Kindle
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Book Description Principles and Practice of Clinical Trial Design is the authoritative textbook on Clinical Research Medicine. The first of a three volume series, this volume addresses key issues in clinical trial design, including patient selection, dosing, and endpoints. This book is intended for physicians and other clinical research professionals in industry, academia, and government institutions. Book Info Boston Academic Publishing. Boston, Massachusetts. Textbook on clinical trial design. Hardcover.

Critical Thinking In Clinical Research

Author: Felipe Fregni
Publisher: Oxford University Press
ISBN: 0199324514
Size: 31.49 MB
Format: PDF, Kindle
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One of the most crucial skills a clinician, scientist, or student can learn is to create, conduct, and interpret the conclusions of a clinical study. Critical Thinking in Clinical Research teaches these fundamentals in four distinct sections, called "units": the first unit focuses on issues surrounding the design of a study such as population, question selection, randomization, and blinding; Unit 2 presents statistical methods such as analyzing data collected, how to present and discuss the data concisely; the third unit covers practical aspects such as methodology, organizational considerations, principles of trial conduct and reporting; and the final unit delves into study designs, providing the advantages and drawbacks of each design style. Each chapter begins with a short introduction, followed by a hypothetical case that challenges the reader to make decisions, to consider pros and cons of specific approaches, and to evaluate options based on specific conditions. Knowing how to critically read and understand scientific papers and to collect, analyze, and interpret research data, which they in turn can then present in their own scientific manuscript makes this book the perfect resource for anyone looking to contribute to the wealth of scientific and medical inquiry.

Starke V Ter Starke T Chter

Author: Meg Meeker
Publisher: MVG Verlag
ISBN: 3864157498
Size: 69.15 MB
Format: PDF
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In einer zunehmend komplexeren Welt ist es für Eltern nicht immer einfach, eine starke, dauerhafte Bindung zu ihren Kindern aufzubauen. Ganz besonders gilt das für die Beziehung von Vätern zu ihren Töchtern. Dabei erklärt Dr. Meg Meeker, die über mehr als 20 Jahre Berufserfahrung in der Behandlung von Kindern verfügt, in diesem wertvollen Buch, wie wichtig gerade das Verhältnis von Vätern und Töchtern ist. Denn um eine starke, selbstbewusste Frau zu werden, braucht jedes Mädchen die Aufmerksamkeit, den Schutz, den Mut und die Weisheit seines Vaters. Meg Meeker verrät die 10 Geheimnisse, die die Beziehung von Vätern und Töchtern einzigartig machen und den Mädchen den bestmöglichen Sprung ins Leben ermöglichen. Aus dem Buch: - Die essentiellen Tugenden, die ein Vater haben sollte, und wie man sie entwickelt - Was Töchter von Vätern über Selbstrespekt lernen können - Die Wichtigkeit von Grundregeln - Wie wichtig es ist, ein Held für seine Tochter zu sein - Die größten Fehler, die Väter machen können - Wie Stiefväter die Rolle übernehmen können

Principles Of Good Clinical Practice

Author: Michael J. McGraw
Publisher: Pharmaceutical Press
ISBN: 0853697906
Size: 67.50 MB
Format: PDF, Docs
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This text aims to be a one-stop source for guidance and checking the rules for proper conduct of clinical trials, as well as providing a historical perspective of the clinical research landscape. Good Clinical Practice guidelines provide an international quality standard for the regulation of clinical trials. They include standards on how clinical trials should be conducted, provide assurance of safety and efficacy of newly developed drugs and protect human rights. Principles of Good Clinical Practice describes the ethical principles and regulatory requirements that influence the current and future conduct of clinical research. As well as providing essential information on clinical trial design and pharmacovigilance, coverage also includes: informed consent; investigator and sponsor responsibilities; site monitoring; institutional review boards and dependent ethics committees; clinical trial registration and reporting; quality assurance; and future implications for good clinical practices. Principles of Good Clinical Practice will be a definitive text for Clinical Development personnel at pharmaceutical companies, Contract Research Organizations (CROs), PharmD and postgraduate pharmacy students, and medical, pharmacy and drug company libraries

Principles Of Clinical Research

Author: Institute of Clinical Research
Publisher: Routledge
ISBN:
Size: 46.12 MB
Format: PDF, ePub
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In an arena which has seen rapid change over the past decade, this work provides a comprehensive and up-to-date guide to the planning, organization and management of clinical trials.

G3p Good Privacy Protection Practice In Clinical Research

Author: Karl-Heinz Schriever
Publisher: Walter de Gruyter GmbH & Co KG
ISBN: 311028328X
Size: 52.95 MB
Format: PDF, ePub
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Establishing ethical and privacy protection aspects in scientific research, especially in medical research, has a long history. Medical data are usually more sensible than other personal data and require therefore an even higher degree of protection than other personal data. In recent research projects genetic evaluations become more and more important and trigger thereby new and continuing activities in the context of data protection. Genetic data as a subset of medical data are the most sensible category of personal data and require therefore the highest degree of data protection. The book provides a systematic and itemized approach to data protection in clinical research including the handling of genetic material, genetic samples as well as derived genetic data and the subsequent secure storage of them. The set up of different kinds of clinical trials having in addition a genetic part, the concept of a genetic informed consent as well as collection schemes of samples are described in detail. Technical requirements and aspects of data protection including pseudonymization and anonymization procedures taking into account ethics committees requirements as well as the underlying legal framework are also presented. Without any exception, all principles and methods presented are best practices, repeatedly applied in different clinical environments and by no means theoretical considerations.

Neuroepidemiology

Author: Lorene M. Nelson
Publisher: Oxford University Press
ISBN: 9780199748877
Size: 25.64 MB
Format: PDF, Mobi
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Neuroepidemiology is the epidemiologic study of neurological conditions. This fine text provides a comprehensive and accessible overview of research methods for conducting epidemiologic and clinical research on these conditions. It is aimed at neurologists, epidemiologists and public health professionals, as well as students of these disciplines. The book has three parts, each emphasizing the unique aspects of studying neurologic disorders. The first focuses on classic principles of epidemiologic and clinical research, including study design, sources of study bias, and methods for assessing the role of environmental and genetic factors in neurologic disorders. The second part covers each of the major neurologic disorders, with an emphasis of the methodologic aspects of studying these disorders and discussion of future research directions. The third part is devoted to clinical and translational research methods, including the design and conduct of clinical trials and prognostic studies, as well as the principles of health services research and evidence-based medicine. This textbook will give neurologists, epidemiologists, and their students the foundation for conducting rigorous epidemiologic and clinical research on neurologic disorders.