Clinical Technologies Solutions
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Patient-First Solutions For Oncology
11/16/2022
Stay connected with your patients and their data by simplifying collection for sites and sponsors while keeping participants safe, comfortable, and engaged from any location.
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IQVIA Safety Notifications
5/20/2020
Now featuring cross-trial functionality, IQVIA Safety Notifications gives sponsors and contract research organizations (CROs) a centralized, simple solution for disseminating, managing, and tracking SUSARs and other safety notifications.
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Suvoda IRT
9/16/2025
A centralized command center for patient randomization and drug supply management—built for today’s complex clinical trials.
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Drive Patient Enrollments With Data-Powered Recruitment Engine
12/13/2024
Generate consistent, successful clinical trial recruitment on repeat with Citeline Connect's multifaceted approach to patient engagement and recruitment.
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Ophthalomogy Qdata® - Delivering Quality Insights
6/25/2025
This platform ingests structured and unstructured EHR data, harmonizes and links it across datasets, and curates it using advanced natural language processing and machine learning.
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Your Partner For Simplified Site Operations And Maximized Returns
11/13/2025
With dedicated CTA Negotiation, Site Payment, and Financial Analysis experts, we reduce site burden and optimize study execution so your team can focus on delivering exceptional research as care.
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Electronic Informed Consent For Clinical Research
2/16/2024
We partnered with leading academic medical centers, sponsors, hospital systems, and site networks to create an eConsent platform that is easy-to-use and minimizes risk.
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Technology And Scientific Expertise To Power Your Program
8/5/2024
Learn how our expertise in eCOA, RTSM, and eConsent solutions can accelerate your drug development program from early phases to regulatory approval.
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Precision-Built IRT Software That Inspires Quick Action
9/17/2025
With the right IRT platform, you can handle inherent complexities and constant change, enabling confident decisions to move life-changing studies forward.
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Medical Writing Software
6/17/2025
Accelerate Medical Writing Without Compromising Accuracy or Compliance
In the fast-paced world of clinical research, the ability to produce, review, and finalize high-quality documents—on time and with full regulatory compliance—is non-negotiable. Ideagen Document Review (formerly known as PleaseReview) is the trusted collaboration and co-authoring platform that enables clinical teams to streamline document reviews, reduce version chaos, and ensure traceable, auditable feedback across the board.