Best Electronic Data Capture (EDC) Software - Page 8

Geminid Systems Trial Explorer

Search and Analyze Clinical Trials for Free

GoResearch.live

Next-generation eCRF & EDC software for faster, audit-ready clinical trials. GoResearch™.live (https://goresearch.live) is a cloud-based eCRF/EDC platform for clinical trials, observational studies, and patient registries. Supporting traditional, hybrid, and decentralized trial designs, it helps research teams move from study setup to compliant, audit-ready data faster. GoResearch™.live combines the simplicity of no-code study design with powerful clinical data management capabilities for studies of any scale. Build and personalize eCRFs in minutes. Capture high-quality data with instant edit checks, intuitive query management, configurable Source Data Verification (SDV) with Risk-Based Approach, and integrated randomization. Seamlessly connect ePRO/eCOA platforms, external data sources, and third-party systems through open APIs. Real-time dashboards, analytics, and customizable reports provide complete operational visibility, enabling faster, data-driven decisions throughout every stage of the study. Hosted on ISO 27001-certified infrastructure and developed under an ISO 9001-certified quality management system, GoResearch™.live is designed to support compliance with ICH GCP, 21 CFR Part 11, EU Annex 11, GDPR, and HIPAA requirements out of the box.

Harbor EDC

Harbor EDC is an electronic data capture platform intended for data collection for clinical trials. Harbor EDC automates the EDC build and source document creation process to get studies started in record time. Harbor also automates source data entry for clinical sites, reducing data entry time by 90% and enabling fully remote monitoring for sponsors. Pricing is predictable and straightforward, without additional fees based on the number of CRFs or fields. Finally, the platform is fully good clinical practice (GCP) and 21 CFR Part 11 compliant, including full audit trails and role-based access, so that the collected data can be used for FDA submissions.

iCapture

Capture the conversations from trade shows and events with intelligent lead capture. iCapture is the fastest and easiest way to capture high-quality leads at a trade show and deliver them directly to your CRM & Marketing Automation Platform. Eliminate manual entry, capture better leads, and win more deals. Easy to use. Every event. Connected to your CRM.

Average Rating: 4.7/5.0

Total Reviews: 101

IMO Core

IMO Core helps clinicians document diagnoses with greater specificity and maintain more accurate, meaningful patient problem lists. Embedded within EHR workflows, clinically curated terminology connects familiar clinical language to standard code systems while coding intelligence helps identify incomplete or inaccurate documentation. Together, these capabilities improve the quality of clinical data captured at the point of care, supporting patient care, coding and reimbursement, risk adjustment, reporting, analytics, and other downstream uses.

Inductive EDC

Inductive EDC is a cost-effective & compliant platform to help you collect, analyse and manage clinical trials data in mammoth quantity reducing your dependency on the paper-based process. IEDC removes all the roadblocks to achieving a seamless data management environment that expedites your study, improves data quality, and complies with regulatory standards. Our 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.

Infinia ML

Infinia ML and its IDP platform help customers and partners tackle their most complex document processing challenges. The platform reads and understands document content like a human being, using prebuilt document processing engines to extract the information of interest automatically. Enterprise leaders and technology innovators trust Infinia ML to deliver value for critical document processing and automation challenges across their organization.

Average Rating: 4.8/5.0

Total Reviews: 4

inProcess Research

inProcess Research is a SAAS platform for turning ideas into results. Stakeholders in research are all invited onto the platform to foster collaboration. Agile adaptation of modern components overcomes barriers to innovation. Research-on-demand automation throughout the SAAS platform minimizes the time and cost of breakthroughs. Executive leadership, subject matter experts, systems engineers, partner investigators, regulatory specialists, and research coordinators work as a team. Integrated research tools are leveraged along a stepwise research lifecycle. Each step includes the resources needed to succeed, and team members know what's expected of them. Teamwork breeds success in this demanding world of research. Each data source is plugged into the inProcess Data Factory in streaming, batch, or on-demand modes. The factory loads, processes, and publishes quality results into analysis, statistics, and machine learning. Research data is now dynamic, managed, and safeguarded. Reusable data objects are cataloged assets to be leveraged over and over again.

InteleShare Research

InteleShare Research™ is a comprehensive image management suite tailored for modern researchers, offering adaptable intake workflows, enhanced accessibility, and specialized tools to manage imaging research data. It centralizes imaging repositories, supports DICOM and non-DICOM file types, and ensures secure, global collaboration through role-based access and a comprehensive exchange network. Key Features and Functionality: - Centralized Access: Establishes a unified imaging repository for streamlined uploads and instant access, consolidating all research data in one secure, easily navigable space. - Automated Anonymization: Provides advanced anonymization features, including native de-identification and DICOM tag morphing, ensuring compliance with data privacy standards. - Streamlined Intake: Offers automated and customizable intake configurations alongside web-based upload options, eliminating the logistical challenges of managing physical data like CDs. - Efficient Trial Management: Enhances clinical trial efficiency with automated intake, routing, and access mechanisms, facilitating digital access and streamlined management of subject imaging data. - DICOM Tag Morphing: Utilizes DICOM tag morphing and wrapping to optimize data intake processes, maintaining the integrity and relevance of subject information. - Secure and Compliant: Ensures secure data handling with native de-identification and anonymization features, supporting stringent data privacy requirements. - Collaboration Portal: Facilitates secure sharing and collaboration on clinical trial data among researchers, partners, and site managers through web-based image share pages and role-based user access. Primary Value and User Solutions: InteleShare Research™ addresses the complexities of managing imaging research data by providing a centralized, secure, and efficient platform. It streamlines data intake, automates anonymization processes, and enhances collaboration among researchers, thereby reducing logistical burdens and ensuring compliance with data privacy standards. This solution empowers researchers to focus on their core work, accelerating the pace of scientific discovery and innovation.

Intely

The ultimate no-code data integrator and custom form building & automation platform. Quickly create enterprise workflows with simple drag-and-drop functions and pre-built tools. Intely offers tailored form creation, data integration, and workflow automation. Easily integrate your stack, consolidate your data, and automate your workflows to get more done in less time.

Intent by Upflowy

Intent by Upflowy generates AI-driven summaries from lead browsing patterns.

Jeeva eClinical Cloud

Jeeva eClinical cloud helps clinical researchers, patient advocacy groups, clinical research organizations (CROs), public health research organizations, and Biopharmaceutical sponsors to accelerate remote patient recruitment by 3x faster by reducing the logistical burdens on patients and study teams by over 70%. This modular software design allows a rapid study configuration with the features and workflows that fit the specific trial protocol whether short-term or long-term, cross-sectional or longitudinal, interventional or observational studies.

Kayentis

Clin’form is a unique fully integrated platform to collect and manage eCOA data in clinical trials. Clin’form offers complementary patient-centric features to support at home and on-site clinical trials. Powerful and customizable, Clin’form can adapt and evolve according to trial specificities, and integrates several services to guarantee trial efficiency as well as support patient engagement. User-friendly, Clin’form simplifies the patients, sites, and sponsors clinical trials experience.

Klindat

KlindatTM is a next-generation electronic Case Report Form (eCRF) for the pharmaceutical, biotech & medical device industries

Kymolog

Kymolog™ is medical device integration and research analytics on the same data. An edge agent beside the devices picks up each reading as the device reports it and writes it as an HL7 FHIR R4 Observation with a LOINC code, a UCUM unit, the device (down to its serial number and UDI) and the time of measurement. Kymolog matches the reading to the patient and encounter by bed and files it in the EHR the hospital already runs: Epic, Oracle Health (Cerner), MEDITECH, athenahealth, eClinicalWorks, NextGen or Veradigm, over FHIR R4 or HL7 v2. The same coded record is kept for research with its device, time, patient and encounter, so a study dataset traces every value to its source. Kymolog reads continuous glucose monitors, ECG monitors, blood pressure cuffs, thermometers and pulse oximeters, and any other device class joins by configuration. The install runs on premises or in its operator's own cloud: a hospital's, or a device maker's when the maker runs it for its hospital customers. The research store runs beside the install or in our cloud, which only receives de-identified readings. An optional data network adds consent, de-identification, dataset licensing and royalties to contributing sites. Kymolog is built for hospitals that want device readings in the chart, device makers who need real-world evidence for post-market surveillance and PMCF, hospital and academic researchers, and trial sponsors running wearables in studies. Request a demo at https://kymolog.com/demo