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Mapping clinical data to CDISC SDTM is mandatory for clinical trial submissions. But accurately mapping to SDTM is increasingly complex and time consuming, especially when it’s done the traditional way with spreadsheets.
You’re repeatedly creating specs from scratch, which is inefficient and leads to inconsistencies and manual errors. Plus, it’s hard to keep track of all the different versions and changes. Managing compliance with evolving regulatory standards is also a mission.
Overall, it’s not a great outcome. There’s a smarter way with Pinnacle 21 Enterprise Plus, the collaborative workspace that transforms SDTM mapping.
With Pinnacle 21Enterprise Plus, you get faster study setups. You can efficiently manage study metadata in a centralized platform. You have complete traceability, and in stream validation allows you to resolve compliance issues upfront.
As a result, you’re looking at faster, higher quality, more consistent submissions, together with greater team productivity.
Streamline your SDTM mapping today.
Visit our website to learn more.
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。
