Central Laboratories Products/Services
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Why Australia Is The Best Place In The World For Early Phase Studies
8/8/2024
The Australian Advantage is about saving time and minimizing costs while generating internationally accepted data in preparation for the next Phase.
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Document Review Integrations And Technology Partners
6/18/2025
At Ideagen, we're committed to empowering seamless collaboration and enhancing your document review process. Through strategic alliances with leading technology providers across the life science industry, we offer integrations that amplify the efficiency and effectiveness of your workflows.
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Digital Transformation Services
8/29/2024
Enabling organizations of all sizes to transform their business through better use of technology.
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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.
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EHR To EDC Connectivity With TrialKit
12/29/2025
Capture EHR/EMR data in TrialKit with no integration required.
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Power Meets User-Centricity With Curebase EDC
8/29/2024
Seamlessly integrated with Curebase’s ePRO/eCOA suite, our EDC enables hybrid and site-based studies that users will love and that streamline all of your data collection into a single, modern experience.
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Medrio EDC Software
5/15/2024
More than just an electronic data collection tool, our robust clinical data management system combines an intuitive user interface, seamless online and offline data capture capabilities, and comprehensive data management for clinical trials in a single solution.
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The SaaS Clinical Data Science Platform
4/8/2024
Signals Clinical streamlines clinical data workflows, reducing the time spent preparing data for analytics. Its comprehensive platform enables the rapid delivery of clinical insights that inform both clinical and operational study decisions.
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Computer Systems Assurance And Validation
7/22/2025
Computer System Validation to cover all your GMP, GLP, GCP, and QA/QC software applications. CompliancePath currently has 30+ active projects globally supporting clients in CSV/CSA compliance.
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Efficiency, Flexibility, And Speed: Building Better Clinical Trials
9/19/2023
Zelta’s EDC has been used in more than 4,000 studies from startup to submission, across all phases, including over 500 phase 3c trials and 23 therapeutic areas.