Best Electronic Data Capture (EDC) Software - Page 5

Catchtrial ePRO/eCOA

Catchtrial® ePRO/eCOA by Medigen Suite is a patient-friendly ePRO software platform for collecting electronic patient-reported outcomes and clinical outcome assessments in modern clinical trials. It delivers real-time symptom diaries, quality-of-life data, and validated instruments directly from patients on any device. Built for sponsors, CROs, biotech, pharmaceutical, and medical device organizations, the platform improves patient engagement, protocol compliance, and data quality. Catchtrial® ePRO/eCOA supports GDPR, HIPAA, ICH-GCP, and 21 CFR Part 11 requirements, helping teams capture reliable patient-reported outcomes across decentralized, hybrid, and site-based studies.

ClinAccess

Comprehensive SAS based clinical data management, EDC, and clinical trials reporting system

ClinicalAnalytics

ClinicalHawk EDC

Electronic Data Capture software streamlines the gathering of trial patient data for early to late-stage clinical research phases, as well as post-approval studies. An adaptable and scalable EDC system is used by Pharma, Biopharma, Medical Device Companies, across the clinical research industry.

ClinicalPURSUIT

Clinion ePRO

Clinion ePRO is a secure platform designed to capture patient-reported outcomes directly from patients in real time. With support for mobile and web access, it enables seamless data collection while ensuring accuracy, compliance, and patient engagement across studies. What can you expect? ● Integrated or Standalone Deployment Use ePRO as a standalone solution or integrate seamlessly with Clinion EDC for unified data flow ● Direct Patient Data Capture Collect responses directly from patients through mobile or web, eliminating intermediaries and reducing data delays. ● BYOD Flexibility Allow patients to use their own devices, improving participation and reducing operational overhead. ● Real-Time Data Validation Validate responses instantly and sync data securely with Clinion EDC or operate in standalone mode. ● AI-Driven Data Checks Compare ePRO and EDC data to identify discrepancies early and reduce manual queries. ● Multilingual and Configurable Forms Deploy customized questionnaires with support for global studies and licensed instruments. Impact Improved patient compliance through reminders and an easy-to-use interface Reduced manual queries with early discrepancy detection Scalable across single-site and global trials

Clinion eSource

Clinion eSource enables site teams to capture clinical data directly at the point of care, reducing manual entry and delays. Built within a unified platform, it ensures accurate, complete, and audit-ready data from the start. What can you expect? ● Direct Data Capture at Source Enter data during patient visits to remove duplicate entry and reduce transcription errors. ● Real-Time Sync with EDC Sync source data directly with Clinion EDC to maintain consistency across systems. ● Faster Study Execution Reduce data cleaning effort and move studies forward with ready-to-use data. ● Reduced Monitoring Effort Enable focused monitoring with real-time visibility into site data. ● Audit-Ready Compliance Maintain full traceability with timestamps and version control aligned with regulations. ● Easy-to-Use Interface Simplify data entry with a clean interface designed for site users. Impact Reduced manual entry and transcription errors Faster database readiness Lower monitoring effort

Clinpal

A new breed of cloud-based, patient-centric data capture solutions designed to handle both ePRO and EDC on BYOD.

ClinVigilant eClinical

Streamline your clinical studies with ClinVigilant, your global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us thanks to our: ♦ Fast EDC set-up (less than 4 weeks). ♦ Cost-effectiveness. ♦ 3rd party integrations (including legacy systems). Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA. The ClinVigilant® eClinical suite includes: EDC, eCRF, CTMS, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem. How simple and user-friendly is it? Ask for a demo to find out! Clinvigilant💊, your one-stop 🌐solutions provider for ☁️clinical trials . Enquiries > bd@clinvigilant.com

Cloudbyz EDC

Cloudbyz EDC is a cloud-native solution with an intuitive interface that is designed to store and manage clinical data effectively throughout a clinical trial’s life cycle. Our innovative solution enables clinical research teams to efficiently collect, analyze, and manage clinical data of different complexity and size. Build your study without code, with an interface that helps users build forms and easily navigate to the appropriate screens for data collection and analysis.

CRFweb

Cronos

Cronos is a clinical trial management software

cubePRO

DADOS

DADOS makes it easy for patients to fill out questionnaires directly on their tablet, from which clinicians and researchers can retrieve this information and build custom reports.

Datacapt

Join the New Clinical Trial Experience. Datacapt is a next-generation unified EDC platform designed for CROs, Sites, Sponsors and Participants in the Medical Device, Biotech and Pharmaceutical industry. Enjoy a modular, easy-to-use and powerful platform for your next on-site, hybrid or decentralized clinical trials. With a clean and intuitive interface, we provide enhanced accessibility, flexibility, and convenience empowering researchers to conduct clinical research efficiently and effectively!