Pull all trial data resources into a single interface. Data visualization, calculated metrics, risk mitigation, site scoring, patient scoring, CRA performance metrics & more.
At Remarque Systems we do not replace your existing systems, we connect them!
Clinical trial software users are familiar with the term ‘single platform’, which often indicates re-configuring massive amounts of data into a centralized system. Remarque Systems platform aggregates any and all data in its current format, allowing it to easily manage legacy data as well as adapting to incorporating new data.
With the flexibility to integrate any data, Remarque’s platform allows analysis and monitoring to be customized to any trial regardless of size. Data integration is complete within weeks, and continuous machine learning improves insights as more data is incorporated.
Remarque Systems currently scores 54/100 in the Clinical Trial category. This is based on press buzz (30/100), recent user trends (falling), and other relevant information on Remarque Systems gathered from around the web.
| The score for this software has stayed the same over the past month. What is this? |
Regional Restrictions: Designed to meet global compliance standards. Completely configurable to accommodate unique needs.
Risk based monitoring in clinical trials was the initial use for the platform when it was created. It has since evolved into a complete oversight tool for clinical trial workflows, operations, data, and compliance.
Our customers continue to find new ways to leverage our system by importing creative data sources into the platform. The ability to created calculated metrics from data points across different systems has made the most interesting question: "What insight can you calculate or come up with?"
It can integrate with any app that has a compatible API or a flat file output.
Yes it does! Contact us for more information on how to become part of our ecosystem.
Contract Research Organizations, Pharmaceutical companies, Sponsors, Consultants, Research Universities, other data source companies (wearables, medical imaging diagnostics, health applications, regulators, and more)
Yes. Users are assigned profiles as well to limit what they can and cannot see, edit, or export.
CTMS, EDC, IVR, Labs, Medical Records, ePRO, wearables, legacy data warehouses, legacy systems, phone apps, any data source with a flat file output or API.
eClinicalWorks, Medrio, Rave, Veeva, Medidata, Parexel, Allscripts, Epic, Cerner, GE Healthcare, Inform Diagnostics, Eclipse, Meditech, Oracle, IBM, and more....
Yes. We have a very experienced team of seasoned professionals that will train you and your teams on how to use our system. Additionally, we have a program to allow you to become qualified for self-help which can become a tremendous savings for your studies over time.
