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Manually designing CRFs and building EDCs causes delays in study setup. CRFs can’t be fully reviewed until the EDC is built, leading to endless revisions and rebuilds, long approval cycles, and delays to study go live.
Using multiple EDCs adds time, cost, and compliance burden, especially having to validate against EDC specific rules. Not forgetting manual updates to versions of CDISC and controlled terminology every quarter.
Meet CRF Creator, a centralized, EDC agnostic platform where you can design, review, and approve eCRFs before study build. Visualize eCRFs exactly as they’ll appear for EDCs and create a library of standardized, reusable assets.
Having standardized eCRFs reduces manual work, speeds review, and boosts compliance. Impact analysis and version tracking provide full visibility.
Now you can work seamlessly across leading EDCs and validate against EDC specific rules. Automated CDISC and controlled terminology updates keep studies compliant.
结果如何？
Quicker study setup, higher quality data, and faster go live.
Visit Certara dot com to learn how CRF Creator can automate your study design and build.
通过 Pinnacle 21 变革临床数据
预约咨询，了解 Pinnacle 21 临床数据管理软件如何加速您从研究设计到提交的进程。
