The CRC's guide to coordinating clinical research /
This guidebook is filled with valuable information on the role and responsibilities of a clinical research coordinator (CRC) and explains the research process from the site and CRC perspective. Topics covered include: identifying the regulations governing clinical research; describing the drug devel...
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Author / Creator: | Woodin, Karen E. |
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Imprint: | Boston, MA : Thomson CenterWatch, ©2004. |
Description: | 411 pages : illustrations ; 23 cm |
Language: | English |
Subject: | Clinical trials -- Standards -- Law and legislation -- United States. Drug approval -- Law and legislation -- United States. Clinical Trials as Topic -- standards -- United States -- Legislation. Clinical Trials as Topic -- legislation & jurisprudence -- United States. Drug Approval -- organization & administration -- United States -- Legislation. Ethics, Research -- United States -- Legislation. Guideline Adherence -- United States -- Legislation. Research Design -- United States -- Legislation. United States. Legislation. |
Format: | Print Book |
URL for this record: | http://pi.lib.uchicago.edu/1001/cat/bib/10142282 |
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100 | 1 | |a Woodin, Karen E. |0 http://id.loc.gov/authorities/names/n2003128249 |1 http://viaf.org/viaf/68313682 | |
245 | 1 | 4 | |a The CRC's guide to coordinating clinical research / |c Karen E. Woodin. |
246 | 3 | 0 | |a Coordinating clinical research |
246 | 3 | |a Clinical research coordinator's guide to coordinating clinical research | |
260 | |a Boston, MA : |b Thomson CenterWatch, |c ©2004. | ||
300 | |a 411 pages : |b illustrations ; |c 23 cm | ||
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500 | |a Readers of this guide can take an online exam to apply for approximately 10 nursing contact hours. Thomson CenterWatch and Thomson American Health Consultants, providers of this continuing education offering, are accredited by the American Nurses Credentialing Center's Commission on Accreditation. | ||
504 | |a Includes bibliographical references. | ||
520 | |a This guidebook is filled with valuable information on the role and responsibilities of a clinical research coordinator (CRC) and explains the research process from the site and CRC perspective. Topics covered include: identifying the regulations governing clinical research; describing the drug development process; discussing good clinical practices and how to apply them in clinical trials and organizing a clinical practice. | ||
650 | 0 | |a Clinical trials |x Standards |x Law and legislation |z United States. | |
650 | 0 | |a Drug approval |x Law and legislation |z United States. | |
650 | 1 | 2 | |a Clinical Trials as Topic |x standards |z United States |v Legislation. |
650 | 2 | 2 | |a Clinical Trials as Topic |x legislation & jurisprudence |z United States. |
650 | 2 | 2 | |a Drug Approval |x organization & administration |z United States |v Legislation. |
650 | 2 | 2 | |a Ethics, Research |z United States |v Legislation. |
650 | 2 | 2 | |a Guideline Adherence |z United States |v Legislation. |
650 | 2 | 2 | |a Research Design |z United States |v Legislation. |
655 | 2 | |a Legislation. | |
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776 | 0 | 8 | |i Online version: |a Woodin, Karen E. |t CRC's guide to coordinating clinical research. |d Boston, MA : Thomson CenterWatch, ©2004 |w (OCoLC)609404364 |
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