Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1094121 | Zeitschrift für Evidenz, Fortbildung und Qualität im Gesundheitswesen | 2014 | 11 Pages |
Abstract
Monitoring in epidemiological studies performed at physicians' offices should be carried out in accordance with the monitoring in clinical trials. On-site monitoring helped to avoid missing data and to ensure adherence to exclusion criteria. On-site monitoring considerably contributed to the correct and complete study inclusion of all eligible participants and a high quality of study data.
Keywords
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Authors
Sylke R. Zeissig, Kathrin Radde, Melanie Kaiser, Maria Blettner, Stefanie J. Klug,