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With significant benefits over traditional, manual data entry methods, Electronic Data Capture (EDC) is quickly becoming the technology of choice. Recent guidance from the FDA promotes capturing source data electronically to ensure the reliability, quality, integrity and traceability of data from the electronic source all the way through to electronic regulatory submission. But that’s just the beginning. In this presentation, delivered by Wim Verreth, our expert in Clinical Data Management, at Outsourcing in Clinical Trials Europe 2014 on May 21-22 in Brussels, Belgium, you can find out how adopting an eSource system in your clinical pharmacology unit can go beyond simple EDC to help you achieve complete clinic automation.