Data integrates from your existing systems! Our platform can enable advanced technology capabilities to your legacy systems and data warehouses.
With data analytics across multiple data sources in your study machine learning provides all stakeholders with insights that are focused on patient safety, process efficiency, compliance and cost control.
Our platform allows analysis and monitoring to be customized to any trial regardless of size. There are a number of features that increase your custom study setup efficiency over time.
What customers are saying:
We set up a FLD to notify us when a site was reaching 8 subjects within a certain age group, as study is age stratified, and we were able to identify an age group that needed to be closed down.
We noticed a trend within a site of not meeting a 24 hour dosing requirement and the site had to be retrained. This affected 4 subjects that had been enrolled and listed as completed, that had to then be listed as early terms.
We noticed a trend within a site of subjects meeting the stop dosing criteria, but dosing continued. This affected 2 subjects that had been enrolled and listed as completed, that had to then be listed as early terms.
Remarque Systems’ capabilities not only meet the ICH guidelines for risk-based monitoring, but can also help companies understand the potential impact of their trials much earlier than traditionally possible.
A single platform for all your clinical trials!