It’s time to deliver flexibility to sponsors, sites, and patients without compromise.
Product Features and Benefits
MANAGE TRIAL SUPPLIES
COLLECT ELECTRONIC CLINICAL OUTCOME ASSESSMENTS
CONSENT PATIENTS
AMPLIFY YOUR PATIENT VOICE
EMBEDDED DATA-DRIVEN INTELLIGENCE
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MANAGE TRIAL SUPPLIES
AMPLIFY YOUR PATIENT VOICE
EMBEDDED DATA-DRIVEN INTELLIGENCE
COLLECT ELECTRONIC CLINICAL OUTCOME ASSESSMENTS
CONSENT PATIENTS
Proven to reduce consent-related protocol deviations by more than 50%, even where e-signature cannot be deployed
The only remote consent solution with true interactive, feature-rich capabilities and a full audit trail
Unmatched ability to scale
Consent patients
Consent patients electronically regardless of geography, regulatory environment, and healthcare setting. IQVIA’s Complete Consent solution is:
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Implements simple to complex randomization and drug dispensation models across all therapeutic areas
Simplifies all trials, even the most complex novel or adaptive trials, ensuring quality and patient centricity
Delivers flexible technology solutions tailored to fit any trial type, business process or integration needs
Drives study savings and decision-making through forecasting and simulation, drug supply optimization tools, industry-leading algorithms, embedded intelligence and analytics
Supports key attributes of DCT including direct to patient shipments and hybrid and fully virtual trials
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Manage trial supplies to sites, local depots, or patient homes without sacrificing drug accountability, traceability, or returns and destruction capabilities. Cenduit’s IRT Solution:
Manage trial supplies
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In-tool capabilities that enable fast setup of all eCOA study activities across multiple devices with simple “drag and drop” functionality
Auto generation of regulatory and project documentation and access to pre-built libraries of assessments that significantly shorten study start-up times
Support for multiple devices to deliver improved patient compliance
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Collect electronic clinical outcome assessments (eCOA) at the source for rapid analysis and remote monitoring. IQVIA’s eCOA solution allows:
Collect electronic clinical outcome assessments
Collect, consolidate, and analyze all data on devices worn or used by patients
Increase the amount and quality of clean, patient-driven data from devices
Provide richer insights with aggregated, verified, continuous data
Support investigators and patients in tracking and analyzing data
Deliver value throughout the study with a Help Desk that supports 215 languages
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Gather biometrics data analytics that is built on eSource technology to seamlessly allow data to flow between connected devices to amplify the patient voice, accelerate outcomes, and achieve confident study goals. IQVIA’s Connected Devices:
Amplify your patient voice
Streamlined data collection from any source into a single ecosystem
Gaining insight into patient behavior to monitor and assess health outcomes
Support of clinical, operational, and real-world analytics
Increase the value of their data by making the right decisions at the right time
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Allow sponsors to generate faster and smarter insights by applying sophisticated machine analysis to subject data investigations, risk management, and performance metrics. IQVIA’s CDAS solution allows:
Embedded data-driven intelligence
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EMBEDDED DATA-DRIVEN INTELLIGENCE
AMPLIFY YOUR PATIENT VOICE
COLLECT ELECTRONIC CLINICAL OUTCOME ASSESSMENTS
MANAGE TRIAL SUPPLIES
CONSENT PATIENTS
