Central Laboratories Solutions
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Risk-Based Monitoring
9/26/2023
Program, country, and study managers, CRAs, clinical monitors, trial managers, clinical data managers, CROs, and others need informatics solutions that help them focus on sites in greatest need, based on risk.
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An EDC/DDC Solution For Modern Clinical Trials
1/16/2024
Utilized in over 3,000 clinical trials, learn about this comprehensive EDC solution that delivers high-quality data on time and addresses any study team's goals.
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Leverage AI To Optimize Protocol Design & Study Start-Up
9/26/2024
Citeline SmartSolutions is an integrated suite of solutions that optimizes and accelerates clinical trial planning and site selection. These AI-enabled technology products help study sponsors reduce costly protocol amendments and increase predictability.
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Revvity Signals Software Solutions For Pharmacovigilance And Drug Safety
5/13/2022
Strategically transform your medical review, safety review, and compliance monitoring processes with our innovative solution for Pharmacovigilance.
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Powering Smarter Treatments And Healthier People
6/19/2024
Explore Medidata's commitment to transforming the life sciences sector, fostering patient-centric trials, and creating new opportunities for healthier populations globally.
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Choose An Oncology Offering Designed Around Patient Experience
Examine this factsheet to see how Medable’s oncology offering simplifies data collection for sites and sponsors while keeping patients safe, comfortable, and engaged from any location.
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Standardized Data In One Place
1/27/2025
Simplify clinical trial data management with Signant’s Clinical Data Hub. Harness machine learning to aggregate diverse data sources, streamline analysis, and unlock timely, actionable insights.
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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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End-To-End Safety Solutions Designed For Success
6/6/2023
As one of the world’s largest and most experienced safety and PV organizations, unearth how this provider is bringing extensive expertise and regulatory intelligence to every industry engagement.
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Rave TSDV - Improve CRA Efficiency And Reduce Site Burden
12/20/2023
Source data verification (SDV) is a critical activity within clinical trial monitoring, yet the traditional approach focused on 100% SDV is limited in its ability to quickly identify issues and prevent them from recurring. Rave TSDV (Targeted SDV), unified with Rave EDC, enables CRAs to focus on critical to quality (CtQ) factors identified within risk management activities.