Total Products under this Category: 136
Last updated: September 11, 2026
Why You Can Trust G2's Software Rankings:
G2's software rankings are built on verified user reviews, rigorous moderation, and a consistent research methodology maintained by a team of analysts and data experts. Each product is measured using the same transparent criteria, with no paid placement or vendor influence. While reviews reflect real user experiences, which can be subjective, they offer valuable insight into how software performs in the hands of professionals. Together, these inputs power the G2 Score, a standardized way to compare tools within every category.
Highlighted products: Medrio EDC, Viedoc, cubeCDMS, Greenlight Guru Clinical, Medidata Rave, Oracle Clinical, Castor, and iMednet EDC.
Underlying data: [Grid® JSON](https://www.g2.com/categories/electronic-data-capture-edc/grids.json?focus%5B%5D=medrio-edc&focus%5B%5D=viedoc&focus%5B%5D=cubecdms&focus%5B%5D=greenlight-guru-clinical&focus%5B%5D=medidata-rave&focus%5B%5D=oracle-clinical&focus%5B%5D=castor-edc-castor&focus%5B%5D=imednet-edc)
EvidentIQ is an innovative software solution that facilitates clinical trial data management and documentation for investigators, sites, CROs and sponsors. EvidentIQ EDC enables electronic data capture across all phases of clinical research with flexible tools allowing you to manage your site infrastructure and workflow efficiently.
Fastrial is ideally suited for start-ups and mid-size companies alike to manage their international trials. Fastrial comes with a set of predefined easy to use libraries. Users can customize and modify these according to their needs. eCRF can be quickly created by using a drag-and-drop interface. Users can create and publish their study with speed and efficiency. Clone their templates to produce unlimited studies with a few clicks. Fastrial is adapted to every budget, thanks to its pay for what you need features.
Florence Healthcare's StudyOrganizer is a powerful product designed to streamline and optimize clinical trial management. This tool supports trial coordinators in efficiently organizing study documents and workflows. For instance, it provides a centralized location for securely storing and accessing essential trial documents, enabling seamless collaboration among team members across multiple sites. StudyOrganizer helps maintain regulatory compliance with audit-ready documentation and offers customizable dashboards for real-time monitoring of study progress. By facilitating clear communication and data exchange with sponsors and other stakeholders, StudyOrganizer supports faster decision-making and smoother trial execution. This product minimizes administrative burdens and enhances efficiency, allowing clinical research professionals to focus on delivering successful trials.
FormsCenter allows you to gather and track data in a clear, consistent and mandated way, whether you are collecting information from external sources, internal employees, or 3rd party software. Integrate all of your software and simplify data entry by easily importing and exporting information and pre-populating fields.
Search and Analyze Clinical Trials for Free
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 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.
Create and use better clinical patient data in your EHR. IMO Core is a problem-oriented clinical workflow solution that simplifies provider documentation and problem list management, while making clinically relevant patient data easily accessible at the point of care.
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.
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™ 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.
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.
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.
KlindatTM is a next-generation electronic Case Report Form (eCRF) for the pharmaceutical, biotech & medical device industries
ArisGlobal’s LifeSphere platform is a suite of unified cloud solutions that helps hundreds of global life sciences companies accelerate development, maintain compliance and streamline collaboration between cross-functional teams. LifeSphere enables the life sciences industry to bring safer products to market more quickly.
