Veeva：2024年如何维护收集临床数据的标准报告（英文版）

As your company grows and runs more trials, reusing case report form (CRF) designs and edit checks can deliver benefits at scale. The increase in efficiency, speed, and quality motivate organizations to develop internal data collection standards1 for their clinical data collection instruments. Yet, these benefits are only possible with consistent enforcement and governance processes in place.

Many data management teams report that their standards initiatives have stalled or failed due t