Newsletter | August 26, 2024

08.26.24 -- Pioneer Clinical Studies' SIP Testimonial

INDUSTRY SOLUTIONS

Pioneer Clinical Studies' SIP Testimonial

CEO and Site Director of Pioneer Clinical Studies Jeff Somerstein tells how Cognizant's Shared Investigator Platform (SIP) has increased his organization's visibility with sponsors.

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Cognizant

Built For Sites To Benefit All

This one-minute video highlights the benefits of One Home for Sites. Join the movement to increase clinical trial capacity, because patients are waiting.

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IQVIA Technologies

StudyIQ Trial Management Suite Overview

Witness how this reporting solution facilitates high-quality clinical data and supports efficient trial management. All reports, dashboards, and analytics come standard with our eCOA solutions.

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Signant Health

Elevate Your Clinical Research Data Collection

By embracing TrialKit’s end-to-end clinical trial data platform, researchers are better enabled to overcome the challenges of non-interventional studies effectively.

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Crucial Data Solutions

How eBinders Can Help With eISF In Europe

By addressing the unique hurdles tied to regulations in European clinical trials, eBinders offer a streamlined approach to managing electronic trial documentation.

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Florence Healthcare

A Site Perspective On Patient Engagement

For a deeper understanding from a clinical site's perspective, hear what this clinician had to say about their experience with Greenphire's solutions and support.

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Greenphire

Linking Clinical Trials To Real World Data

Clinical trial data (CTD) and RWD can be linked through Medidata Link at the participant level, enhancing the generation of evidence beyond what is possible in conventional clinical trials.

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Medidata AI

A Powerful Platform That's Easy To Use

This unified platform offers streamlined and reusable workflows, user-friendly interfaces, and transparent dashboards that enhance the user experience and overall outcomes.

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OpenClinica

Real World Data Solutions

Leverage Citeline RWD Solutions to enhance feasibility assessments, select optimal trial sites from the start and, when necessary, support trial rescue efforts.

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Citeline