Healthtech > Clinical Research Data Software
Launch a Clinical Research Data Software in as fast as 2 weeks
Design, build, and launch your clinical research data software fast & right with AI
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Building a custom Clinical Research Data System allows you to create recruitment workflows that integrate with your EHR, implement protocol templates specific to your research focus, and build data collection forms tailored to your study designs. A custom solution enables you to conduct research more efficiently whilst maintaining complete control over research data and ensuring compliance with institutional and regulatory requirements.
Building a custom Clinical Research Data System allows you to create recruitment workflows that integrate with your EHR, implement protocol templates specific to your research focus, and build data collection forms tailored to your study designs. A custom solution enables you to conduct research more efficiently whilst maintaining complete control over research data and ensuring compliance with institutional and regulatory requirements.
The ROI for a Clinical Research Data System comes from accelerated trial recruitment (typically 50-60% faster), reduced protocol violations through systematic compliance monitoring, and lower regulatory submission costs through automated documentation. Research organisations see substantial improvements in trial completion rates alongside better data quality, whilst reducing the administrative burden that often delays research progress.
There's a range of features you can build for your custom a Clinical Research Data System�it really depends on your specific needs and patient population. But we've rounded up some of the essential features that make a Clinical Research Data System effective and valuable.
Screen EHR data to identify potentially eligible patients with automated outreach and consent tracking. This proactive recruitment accelerates enrolment whilst ensuring systematic screening that doesn't miss eligible patients.
Track adherence to study protocols with automated alerts for missed visits, medication compliance, and required assessments. This monitoring prevents protocol violations whilst ensuring complete data collection that supports valid research conclusions.
The ROI for a Clinical Research Data System comes from accelerated trial recruitment (typically 50-60% faster), reduced protocol violations through systematic compliance monitoring, and lower regulatory submission costs through automated documentation. Research organisations see substantial improvements in trial completion rates alongside better data quality, whilst reducing the administrative burden that often delays research progress.
Hop on an exploratory call and find out how we can accelerate your software project, best for innovators looking to find a build partner for their new product ideas.
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