Sunday, July 10, 2011

Clinical Research

Clinical Research



Author:
Edition: 1
Publisher: Lippincott Williams & Wilkins
Binding: Paperback
ISBN: 1605477486



Clinical Research: From Proposal to Implementation


Clinical Research: From Proposal to Implementation will serve as a road map for students and junior researchers seeking to successfully design, implement, and publicize the results of clinical research. Medical books Clinical Research. The book covers the basic elements of research proposals and implementation including regulatory approvals, continuing regulatory oversight, monitoring patient safety, recruitment, clinical assessments, laboratory assessments, provision of treatment, and on-going quality control. It familiarizes readers with the regulatory aspects of human research and the procedures involved in investigational new drug and device applications. The authors provide a working knowledge of how to integrate research resources to successfully conduct a clinical research project, and offer guidelines on the collection, quality control, and analysis of research data.

A companion website will include the fully searchable text and links to Journal of Investigative Medicine's "Research Tools and Issues" feature Medical books Small Clinical Trials: Issues and Challenges. Categories: Clinical trials. Contributors: Committee on Strategies for Small-Number-Participant Clinical Research Trials - Author. Format: Paperback

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Categories: Clinical trials. Contributors: Committee on Strategies for Small-Number-Participant Clinical Research Trials - Author. Format: Paperback

Categories: Clinical trials. Contributors: Committee on Strategies for Small-Number-Participant Clinical Research Trials - Author. Format: Paperback

Categories: Medicine->Research->Methodology, Clinical Trials->methods. Contributors: Daniel P. Schuster - Editor. Format: Hardcover

Categories: Clinical trials, Biomedical Research->methods. Contributors: Michael J. McPhaul - Editor. Format: Paperback



Medical Book Clinical Research



The book covers the basic elements of research proposals and implementation including regulatory approvals, continuing regulatory oversight, monitoring patient safety, recruitment, clinical assessments, laboratory assessments, provision of treatment, and on-going quality control. It familiarizes readers with the regulatory aspects of human research and the procedures involved in investigational new drug and device applications. The authors provide a working knowledge of how to integrate research resources to successfully conduct a clinical research project, and offer guidelines on the collection, quality control, and analysis of research data.

A companion website will include the fully searchable text and links to Journal of Investigative Medicine's "Research Tools and Issues" feature.



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