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| home > ebr > winter 2003 > the most important current and future data management tasks ahead |
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 PUBLICATIONS |
European Biopharmaceutical Review
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| For over 15 years the industry has discussed how to improve the process of capturing data in clinical trials. A lot of time and money have been invested in finding better ways of preparing data for high quality analysis immediately after the last patient has completed the trial. Most important are data standardisation and systems for entering data at the clinics, or systems whereby patients enter self-reported data. There are many good examples of that usage, but there are still a few trials not using paper CRFs and traditional data entry. While the requisite data standards are not in place, they could save time and money. |
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Industry Events |
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