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Scholar Results 1 - 2 of 2 citing Santiago: Tracking adverse events in RCTs: lack of agreement among regulatory institutions. (0.09 sec) 

Standardizing assessment and reporting of adverse effects in rheumatology clinical trials II …

- ►jrheum.com [PDF] 
T Woodworth, DE Furst, R Alten, C Bingham, D … - Journal of rheumatology, 2007 - jrheum.org
Woodworth, et al: Rheumatology Common Toxicity Criteria v.2.0 ... Personal
non-commercial use only. The Journal of Rheumatology Copyright © 2007. All
rights reserved. ... ABSTRACT. Objective. The OMERACT Drug Safety Working ...
Cited by 1 - Related articles - BL Direct - All 8 versions

►Serious adverse events in academic critical care research


D Cook, F Lauzier, MG Rocha, MJ Sayles, S … - Canadian Medical Association Journal, 2008 - ecmaj.com
Accurate and transparent reporting of serious adverse events in randomized
trials is crucial to evaluating the benefits and harms of various health care
interventions. The Guideline for Good Clinical Practice 1 of the ...
Cited by 1 - Related articles - BL Direct - All 14 versions


 

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