TY - BOOK
T1 - Clinical research
T2 - From proposal to implementation
AU - McPhaul, Michael J.
AU - Toto, Robert D.
N1 - Publisher Copyright:
© 2011 by LIPPINCOTT WILLIAMS & WILKINS, a WOLTERS KLUWER business.
PY - 2012/1/1
Y1 - 2012/1/1
N2 - Publisher’s Note: Products purchased from 3rd Party sellers are not guaranteed by the Publisher for quality, authenticity, or access to any online entitlements included with the product. 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. 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.
AB - Publisher’s Note: Products purchased from 3rd Party sellers are not guaranteed by the Publisher for quality, authenticity, or access to any online entitlements included with the product. 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. 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.
UR - http://www.scopus.com/inward/record.url?scp=85050224109&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85050224109&partnerID=8YFLogxK
M3 - Book
AN - SCOPUS:85050224109
SN - 1605477486
SN - 9781605477480
BT - Clinical research
PB - Wolters Kluwer Health Adis (ESP)
ER -