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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
Deploy Faster, Capture Better Data, and Accelerate Your Research Castor EDC/CDMS empowers research teams to quickly build studies, integrate diverse data sources, and ensure high-quality, compliant, and reusable data. Designed for global scalability, Castor simplifies study setup and streamlines data collection from EHRs, wearables, ePRO/eCOA, and more—reducing errors and breaking down data silos. Quick facts: ? Over 90% of studies with Castor are deployed within 4 weeks—without extensive training. ? Supports clinical trials in over 90 countries, enabling global collaboration. ? Rated 4.7/5 stars on Capterra for ease of use and functionality. ? Seamlessly integrates with EHRs, wearables, and other data sources for a connected ecosystem. ? Fully compliant with FDA 21 CFR Part 11, ICH-GCP, HIPAA, and GDPR regulations.
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.
Your Site's Preferred EDC System. This Electronic Data Capture System (EDC) provides automation for sponsors, CROs, DM's, and more.
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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.
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.
Unify patient, clinician, and device data in one platform. Castor ePRO streamlines data collection by enabling researchers to design, edit, send, and collect complex surveys in minutes—all within a single, centralized system. Our ePRO/eCOA solutions, paired with the Castor Connect app, boost patient engagement while reducing administrative burden. Participants can complete surveys online or offline on their preferred devices, ensuring seamless data capture. With automated scheduling, real-time monitoring, and built-in validations, Castor ePRO makes it easier than ever to gather high-quality, regulatory-compliant patient-reported outcomes. Quick facts: ? 98% customer satisfaction score. ? 40% higher patient retention in trials using Castor. ? 21+ field types, pre-built templates, and advanced validations for survey design. ? Secure, compliant, and fully integrated with EHRs, wearables, and other data sources.
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
Comprehensive Electronic Data Capture Software: - CRF creation and data entry - Support for complex, multi-center studies - Accelerates data validation and processing - Multilingual capabilities - Connects to EDC Mobile, RTSM and ePRO Ennov EDC is a comprehensive clinical data management solution that allows clinical research personnel to easily define EDC studies and collect subject data without the worry of missing or inaccurate data. Ennov EDC is easy to use and supports the design, deployment and capture of multi-center clinical trial data within one flexible and scalable solution. Our software supports clinical trials of any size, including large global trials, post-marketing trials, cohort trials, health surveillance, Phase I-IV trials and epidemiological trials. Ennov EDC facilitates complete and accurate data collection and improves communication within clinical teams.