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Software used to manage clinical trial data electronically. - Capture, store, and validate trial data in a computerized system - Improve data quality, reporting, and regulatory compliance - Share, review, and export data in an electronic format
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Right-Sized eTMF Solutions Whether your eTMF requirements are bite-sized or globalized, IQVIA has a solution to fit your needs. Keep studies on track and compliant with one of IQVIA’s right-sized eTMF solutions. IQVIA eTMF: Proactively reduce risk, increase efficiency, and minimize manual processes with the most advanced eTMF platform available today. IQVIA eTMF is the right solution to take control of compliance and deliver seamless inspections. IQVIA eTMF Essentials: Realize the benefits of owning a comprehensive eTMF platform, including dashboards and an enhanced user experience, without the resources required to implement and administer. IQVIA eTMF Essentials is the right solution when conducting a small number of studies or studies with only a few sites. IQVIA eArchive: Remain inspection-ready beyond database lock and protect investments in completed trials with a simplified and easy-to-use solution. IQVIA eArchive drastically reduces the cost to comply with ICH GCP, FDA, an
Minimize build time, capture better data, and accelerate your research. Castor’s data platform enables every researcher and study team worldwide to capture high-quality, compliant, reusable data. It ranks among the top 5% EDCs, accelerating your study deployment, integrating data from your ecosystem of wearables, devices, eSource, and more, and minimizing data entry error during your studies. Designed to help all users collect and exchange data to deliver better healthcare outcomes, Castor EDC will help research teams digitize the study protocol, integrate your eClinical ecosystem and break data silos. Quick facts: • Over 90% of studies with Castor are deployed within 4 weeks (without the need for extensive training). • Castor supports clinical trials in over 90 countries. • 4.7/5 star rating on Capterra for Castor EDC.
Centralized data right from the patient. Castor ePRO unifies clinician, patient, and device data in a single platform, enabling you to design, edit, send, and collect complex surveys in minutes. Increase patient engagement, relieve administrative burden, and improve data collection with Castor ePRO/eCOA solutions and native Castor Connect app. Empower your study subjects with both online and offline questionnaires on their preferred device and browser. Castor makes it faster and simpler than ever to create, schedule, and send in-app surveys, while viewing their status in real time. Quick facts: • Castor has a 98% customer satisfaction score. • Clinical trials with Castor have 40% higher patient retention. • With Castor ePRO, reuse existing surveys and create complex surveys using more than 21 field types, pre-built templates, and validations.
Clinvigilant Electronic Data Capture (EDC) platform offers a cutting-edge solution for efficient and compliant clinical trial data management. This platform streamlines data collection, entry, and monitoring, enhancing the overall clinical trial process. Its user-friendly interface facilitates seamless data input and retrieval, promoting accuracy and reducing errors. Clinvigilant EDC platform ensures real-time data access, enabling swift decision-making for research teams. With advanced security measures, it safeguards sensitive patient information, ensuring compliance with regulatory standards. The platform also supports remote monitoring, promoting flexibility in study oversight. Overall, Clinvigilant EDC platform optimizes clinical trial workflows, promoting data integrity, security, and efficiency throughout the research lifecycle.
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eTMF Connect is the leading Electronic Trial Master File platform for growing small & medium-sized organizations. Through innovative and modern technology it helps life science organizations better manage their clinical trial documentation, providing real-time inspection readiness and visibility into Trial Master File planning. Aligned with the TMF Reference Model and other industry best practices and models to centralize and standardize clinical records management for emerging biotech, pharmaceutical and CRO organizations.
Greenlight Guru Clinical is MedTech's leading EDC software. Collect and manage clinical data in pre- and post-market clinical studies, including registries, cohorts, surveys, human factor testing, design validation, and more.
More than just an electronic data collection (EDC) tool, Medrio’s clinical data management system (CDMS) combines an intuitive user interface, seamless on and offline data capture capabilities, and comprehensive data management in a single solution. What can you expect? - Quick mid-study changes, no need to rely on tech support or take your study offline. - Allow approved individuals to access your data from multiple devices in multiple locations at any time of day - Ensure your data is entered quickly and accurately by using form rules like edit checks and skip logic
Inductive EDC is a cost-effective & compliant electronic data capture software to help you collect, analyse and manage clinical trials data in mammoth quantity reducing your dependency on the paper-based process. Inductive EDC removes all the roadblocks to achieving a seamless data management environment that expedites your study, improves data quality, and complies with regulatory standards. Our (Electronic Data Capture) EDC system allows you to configure the CRFs for any specific need including academic, biotech, and pharmaceutical study. It ensures greater data privacy and security, along with inherent compliance.
Decentralized and modular – the digital platform for hybrid clinical trials. Our solutions (EDC, ePRO, eCRF, eSurvey and eConsent) enable you to collect clinical data in a decentralized, automated and secure way. Benefit from faster implementation, improved data quality and better patient engagement.