
DCT / Clinical Solutions
Providing expertise from clinical through commercial
Clinical Challenges
The number of drugs approved per billion dollars spent is at an all time low, all the while R&D costs are exponentially increasing, and will continue to do so.
Our Solution
​A unique combination of compliant, scalable, flexible, and interoperable solutions that supports your clinical journey from the lab to engagement.


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Patient Home
Patient Home
Mobile Clinic
Patient Home
Lab Facility
Lab Facility
Mobile Clinic
CLINICAL-IQ™
Achieve patient-centric Clinical Trial management with DCT supported solution to maximize patient participation
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Full multi-channel remote trial management
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Automation to streamline recruitment & enrollment
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Configurability - rapid adaptation to specific protocols
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Dynamic HCP and Patient Portals
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eRecruitment - pre-screening surveys & screening workflows
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Full operational reporting
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HIPAA & 21 CFR 11 Compliant Site Initiation
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eCOA, ePRO, EDC, and CTMS integration
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eConsent embedded in patient engagement workflows
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Integration & data standardization of Clinical Trial ecosystem
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Customizable Data capture from any location



CLINICAL-IQ™
End-to-end clinical trial support
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Digital Lab Sample Management
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High-throughput Screening
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Clinical supply chain management
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Logistics tracking and control
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Complex data analytics
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Transparency reporting and forecasting
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Grants payment management workflows
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21 CFR Part 11 validation and GDPR compliance support
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Data standardization - centralized views of disparate data sources


​Coordinated patient-centric journeys
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Unified front end for a seamless study experience for patients and study staff
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Digital Automation of recruitment and study workflows
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Decentralized and Remote trial support
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Surveys, outreach and patient satisfaction tracking
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Full scheduling capabilities and survey management
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Patient relationship management
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Multi-channel patient/caregiver reminders.
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Interactive Dashboards allow study staff to track enrollment, compliance and monitor adverse events



CLINICAL-IQ™


Compress study timelines and accelerate outcomes.

Corporate Headquarters
855-751-5527