Research

SaaS CLINICAL RESEARCH

Get new drugs to market faster with help from our Clinical Transformation Services practice.

 

Drug companies need to conduct clinical trials faster and more cost effectively. We offer a suite of clinical transformation services and remote monitoring tools that help improve clinical monitoring methods, reduce costs and ensure data quality. Our Clinical Transformation Services leverage the right people in the right roles—and use the latest cloud and mobility solutions to increase productivity. According to benchmark industry data, companies that implement Xeeor’s eClinical Trial Management suite can reduce trial cycle time by more than 20 percent.

Capabilities

 

Clinical Center of Excellence
E-CLINICAL SUITE
Our Clinical Center of Excellence (CoE) ensures tight alignment of the latest technologies with key clinical processes, such as electronic data capture (EDC), clinical data management systems (CDMS), interactive voice or web response technologies (IVRS/IWRS), clinical trial management systems (CTMS) and clinical drug supplies management systems (DSMS). With our eClinical Suite for pharmaceutical companies, the following systems are integrated on a single platform:

• Clinical trial management systems
• Electronic data capture
• Drug supplies management systems

BPS AND RELATED SERVICES

Our metrics-driven service delivery guarantees efficiencies through continuous improvement methodologies including Six Sigma and BPM/BPR. Leading life sciences players turn to us to keep their clinical systems on the industry vanguard.

Highlights include:

• BPS services such as study setup, edit check programming, data extraction and reporting
• Custom application development, upgrades, migration and integration
• Application support and maintenance
• Clinical systems software validation and testing (as per 21CFR11)
• Vendor and/or product evaluation
• eClinical technology and IT strategy roadmaps

 

XeClin®

E-CLINICAL SOLUTIONS

Biomedical organizations, especially the companies working with human study subjects are required to comply with healthcare regulatory guidelines such as US FDA 21CFR, CGMP and HIPAA.

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XEEOR ® LIMS

ENTERPRISE LABORATORY & BIOINFORMATICS PLATFORM

Xeeor’s Enterprise Laboratory Platform encompasses all of the traditional LIMS and ELN concepts and extends them even further by adding complementary capabilities and technologies.

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BUILT YOUR CLOUD

 

Includes all Xeeor Cloud Products and the ancillary services to enhance them.

 

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