Featured Products & Services
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Flexible And Simplified Consent Management
7/31/2025
Learn about a unified ecosystem integrating eConsent, IRT, eCOA, and ePatient into a seamless workstream designed with a patient-centric approach.
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Hybrid eConsent: Remote And On-Site
3/21/2025
Studies show when participants are informed and comfortable with the consent process, they're more likely to comply with protocol, remain enrolled, and contribute to faster study deployment.
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Streamline Your Regulatory Process
1/18/2022
The Advarra eRegulatory Management System (Advarra eReg) provides integrated protocol, staff, and institution documentation to streamline regulatory process and enhance compliance.
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The Cognizant® Shared Investigator Platform (SIP) Document Exchange Module
9/8/2021
The clinical trial process requires effective collaboration and exchange of critical documents between sponsors and sites, but manual methods are burdensome and costly. Cognizant SIP Document Exchange enables seamless collaboration between sponsors and sites for management and exchange of critical study documents.
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Starting A New Study? This One's For You
10/15/2025
Choosing the right vendor at trial launch impacts costs, timelines, data integrity, and patient experience — yet vendor selection in clinical research remains fundamentally broken today.
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Sensors and Wearables: Gain Deeper Insights
6/17/2024
Collect valuable data on treatment effects beyond clinic visits and without burdening patients or sites using mobile health sensors and wearables with secure data collection.
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Harnessing Data For Deeper Insights In Medical Information
2/6/2025
Discover the groundbreaking software solution that your organization can leverage to meet industry demands by transforming vast amounts of raw data into actionable insights.
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Cognizant® Shared Investigator Platform Video Meetings
10/29/2020
The integrated video meetings capability in Cognizant® Shared Investigator Platform (SIP) provides a new way forward for sponsors, facilitating decentralization by consolidating virtual meeting capabilities with other day-today trial activities into a single platform, providing a live connection between sponsors and sites and improving overall trial efficiency.
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Industry-First eTMF AI Reduces Risk Of Document Misfiles And Metadata Errors
4/6/2023
PhlexTMF offers the industry’s only next-generation eTMF AI, providing expert suggestions at the critical document upload step, reducing errors, and improving TMF quality, completeness, and timeliness.
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User Acceptance Testing (UAT): Keeping Trials On Track
12/5/2025
Validate endpoint performance and security before deployment with structured UAT that reduces risk, ensures compliance, and enhances user experience through real-world testing.