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Performing Source Data Verification (SDV) in a clinical trial involves comparing the data recorded on the Case Report Form (CRF) or electronic equivalent (e.g., eCRF) with the original source documents to ensure accuracy, reliability, and compliance with regulatory requirements. The aim of SDV is to look for three (3) things: Data errors Procedural errors Fraud […]
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Implementing decentralized clinical trials (DCTs) involves leveraging digital health technologies and adapting trial processes to enable remote participation and reduce the need for physical site visits[1]. Here are some steps to consider when implementing decentralized clinical trials: Planning and Design: Strategically plan and design the trial to incorporate decentralized elements. Consider factors such as the […]
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