Clinical Technologies Solutions
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Driving Success In Dermatology Drug Development
Our dedicated teams are led by in-house, board-certified dermatologists who have decades of experience conducting early and late phase studies. Download the available brochure to learn more.
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Clinical Data Review Analytics Solution
The Revvity Signals Software Clinical Data Review Solution provides the most effective way to perform an in-depth review of study data, empowering clinical development teams to make smarter decisions faster.
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Implement A BYOD Strategy For Your eCOA Trial
8/14/2023
Delve into the benefits of implementing a "Bring Your Own Device" strategy into eCOA trials.
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ePRO Element
7/27/2022
As industry experts, MRN has delivered innovative solutions using specialized expertise and creative approaches, providing in-home clinical trial visits through their Home Trial Support service to over 230 trials.
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Improve TMF Management And Inspection-Readiness With PhlexEview eTMF
1/27/2021
PhlexTMF embeds TMF best practices and advanced AI technologies proven in life sciences. As the leader in TMF best practices from planning and document management to compliance and archiving, Phlexglobal is at the forefront of innovation in Trial Master File software and services.
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Use Our Experts For eTMF Management, Monitoring, And Maintenance
3/14/2023
IQVIA eTMF Expert Services provide on-demand resources to help manage, monitor, and maintain eTMFs. Dive into the ways these services can improve productivity and ensure compliance.
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TA Scan
1/27/2023
TA Scan is a clinical and commercial intelligence solution that aggregates global clinical trial, presentation, and publication data into a single intuitive database.
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A Modern EDC/DDC For Modern Trial Designs
8/4/2023
This EDC and DDC solution has supported over 3,000 clinical trials over 30 years. Experience the simplicity, flexibility, efficiency, and superior service you’ve been missing from your EDC.
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Unified Platform Solutions For Phase I Clinical Trials
3/19/2024
Phase I clinical trials need technological solutions that support rapid implementation and end-to-end processes. Signant’s unified eClinical platform provides the perfect partner for Phase I research.
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IQVIA Feasibility
9/27/2022
Employing a digital, data-first strategy, IQVIA Feasibility brings together survey data, confidential disclosure agreements (CDAs) and site intelligence data, enabling sponsors to efficiently collect vital information while improving the site experience.