Patient Data Reporting Solutions
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Bridging The Gap Between EHR And EDC
5/19/2025
Clinical trial sites have long relied on manual, error-prone processes to transfer patient data from EHRs into EDC systems, but integrated solutions make streamlining this workflow quick and simple.
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Rave eTMF - Simplify Trial Oversight With Unified Document Management
1/2/2023
Your Trial Master File (TMF) complexity is growing. It’s not uncommon to upload thousands of documents per day, subject to strict regulatory requirements for filing, and under aggressive timelines. Rave eTMF is a global, secure collaboration platform to seamlessly manage Trial Master File content so it is always contemporaneous with the study.
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A Modern Tool For Coding Clinical Data
2/23/2023
Discover how the Anju AutoEncoder solution provides coding consistency across trials, group trials, and entire organizations.
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Medable eCOA
5/26/2022
Medable eCOA is designed to enhance your decentralized trial capabilities with all features native to the platform. Modular by design, use what you need, not what you don’t.
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PhlexTMF: Software For CROs
2/17/2021
Phlexglobal’s PhlexTMF for CROs software is the ideal eTMF for Contract Research Organizations, incorporating innovation based on input from our worldwide customers – both sponsors and CROs – addressing the eTMF business challenges they face every day. The result is purpose-built eTMF software that our customers rely on to develop and implement TMF best practices throughout their organizations, and to ensure effective sponsor-CRO communication and collaboration.
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Powering Urologic Research With Exclusive Real-World Data
6/25/2025
These high-quality, fit-for-purpose data modules are tailored to conditions such as prostate cancer, benign prostatic hyperplasia (BPH), non-muscle invasive bladder cancer (NMIBC), and more.
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A Clinical Research Toolset That Delivers Power And Ease Of Use
1/23/2024
Improve experiences and outcomes in clinical trials with a robust, and modern toolset of best-in-class solutions for eSource, ePRO, data capture, reporting, and more.
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How A COVID-19 Clinical Trial Used Technology For Successful eSource Data Capture
4/19/2022
Transcribing data sucks! But clinical research coordinators must manually transcribe patient data. It’s extremely inefficient, time consuming and highly error prone. Now imagine a world where, in a single click, you can get EHR data into your study database.
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Medidata eConsent – Empowering Patients Right From The Start
8/2/2021
Medidata’s eConsent is an innovative, patient-friendly, electronic informed consent and patient enrollment system for clinical trials. Through the use of multimedia technology, your patients are educated and guided through understanding key elements of a clinical trial.
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How Can Phase 1 Trials Employ eClinical Solutions?
1/8/2024
Uncover how this unified platform is helping sponsors and CROs generate high-quality data, accelerate trials, and rapidly scale to Phase 2 and beyond.