Veeva：2023年临床数据工作台：不断发展的产品类别可加快获取质量数据的速度报告（英文版）

Any clinical trial is only as valid as the data that supports it. Today, establishing that validity is more difficult, since 70% of the patient data used in most trials comes from a diverse range of external sources, including labs, wearable devices, and electronic patient-reported outcomes (ePRO) solutions. It does not fit neatly into a CRF and cannot be managed in an EDC, challenging data managers to find and resolve inconsistencies quickly or efficiently. So far, companies have responded b