Published in TB and Outbreaks Week, February 28th, 2006
In a recently published report, investigators in France conducted a study to "assess the feasibility of coding with MedDRA, the Medical Dictionary for Regulatory Activities, not only serious adverse events required for notification but also all other events usually reported in HIV clinical trials" and to "develop an approach for MedDRA implementation within an institutional research unit that contributes to an efficient, concise and reproducible event coding."
"To evaluate the impact of the maintenance and the versioning of this new medical terminology," MedDRA "versions 3.0 and 5.0...
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