--- title: "Catchtrial EDC+ Software Pricing, Alternatives & More 2026 | Capterra" description: "With the help of Capterra, learn about Catchtrial EDC+ Software - reviews, pricing plans, popular comparisons to other Clinical Trial Management products and more." source_url: "https://www.capterra.com/p/132959/Catchtrial/" page_type: "product" language: "en" --- # Catchtrial EDC+ Software Review 2026: Features, Reviews, Integrations, Pros & Cons Last updated on August 26, 2026 Provider data verified by our Software Research team, and reviews moderated by our Reviews Verification team. [Description](#description)[Use cases](#use-cases)[Alternatives](#alternatives)[FAQs](#faqs)[Features](#features)[Pricing](#pricing)[Support](#support)[Reviews](#reviews) Catchtrial EDC+ ## What is Catchtrial EDC+? Catchtrial® EDC+ is a next-generation clinical trial platform combining data capture, imaging, safety workflows, and AI-driven analytics in one integrated, secure environment. It enables real-time oversight, faster decision-making, and the delivery of high-quality, approval-ready data across global studies. Catchtrial® EDC+ serves as an intelligent clinical trial governance environment, where investigators, core labs, safety adjudication teams, monitors, and statisticians collaborate around real-time data — accelerating the delivery of reliable clinical outcomes. ## What is Catchtrial EDC+ used for? [Clinical Trial Management](https://www.capterra.com/clinical-trial-management-software/)[Electronic Data Capture](https://www.capterra.com/electronic-data-capture-software/) Top alternative Featured Overall rating Based on 1 user reviews Reviews sentiment Positive \- Neutral \- Negative \- Contact vendor for pricing Free trial available Free version not included Capterra Shortlist charts the highest-rated and most popular products... Our "Best of" badge program showcases products with the highest ratings... Our "Best of" badge program showcases products with the highest ratings... Do you work for Catchtrial EDC+?[Manage this product listing](https://www.g2.com/products/catchtrial-edc/claim_requests/new?auto=true) ## Catchtrial EDC+ Overview Updated August 2026 AI summary Catchtrial EDC+ equips organizations of all sizes with tools for managing clinical trials and electronic data capture, supporting compliance with 21 CFR Part 11 and HIPAA. It offers features for study management, patient tracking, document control, and workflow coordination, along with options like audit trails and randomization. The platform is accessible via cloud and multiple desktop environments. ## Compare with a popular alternative Capterra selects software alternatives based on relevant features, verified user reviews and user interactions. Placement may be influenced by client status. ### Catchtrial EDC+ 5.0 (1) VS. [4.7 (204)](https://www.capterra.com/p/143532/Castor-EDC/reviews/) Starting Price Contact vendor Starting Price Contact vendor Free Trial Free Version Pricing Options Free Trial Free Version Ease Of Use 4.0 (1) Ease Of Use 4.7 (88) Value For Money 4.0 (1) Value For Money 4.6 (78) Customer Service 4.0 (1) Customer Service 4.7 (86) ## Catchtrial EDC+ alternatives [4.2 (118)](https://www.capterra.com/p/192454/Research-Manager/reviews/) Starting price Contact vendor for pricing Pricing Options Free Trial Free Version User Rating 86% of reviewers rated it above 4 stars Highest Rated [4.9 (68)](https://www.capterra.com/p/126679/RealTime-CTMS/reviews/) Starting price $500.00 Per User, Per Month Pricing Options Free Trial Free Version User Rating 100% of reviewers rated it above 4 stars [Greenlight Guru Clinical](https://www.capterra.com/p/152998/Greenlight-Guru-Clinical/) [4.4 (88)](https://www.capterra.com/p/152998/Greenlight-Guru-Clinical/reviews/) Starting price Contact vendor for pricing Pricing Options Free Trial Free Version User Rating 95% of reviewers rated it above 4 stars [Learn More](https://www.capterra.com/p/152998/Greenlight-Guru-Clinical/) [Viedoc](https://www.capterra.com/p/160680/Viedoc/) [4.4 (95)](https://www.capterra.com/p/160680/Viedoc/reviews/) Starting price Contact vendor for pricing Pricing Options Free Trial Free Version User Rating 93% of reviewers rated it above 4 stars [Learn More](https://www.capterra.com/p/160680/Viedoc/) ## FAQs about Catchtrial EDC+ Overview ### What company size and specific industries is Catchtrial EDC+ built for? Catchtrial EDC+ is designed for sponsors, CROs, biotech companies, medical device manufacturers, and research organizations of any size running Phase I–IV clinical trials that need secure electronic data capture. Features and Usability ### What are the key features of Catchtrial EDC+? Catchtrial EDC+ offers electronic data capture, data capture and transfer, data import/export, and data verification for clinical study management. It also includes audit trail, 21 CFR Part 11 compliance, HIPAA compliance, document management, workflow management, patient management, patient recruiting, randomization, scheduling, monitoring, and EMR/EHR support. Getting Started and Support ### What training and onboarding options does Catchtrial EDC+ offer? Catchtrial EDC+ provides in person training, live online sessions, webinars, and documentation. In person and live online formats support guided instruction, webinars offer group-based learning, and documentation gives written reference material for self-paced review and feature lookups. Getting Started and Support ### What customer support options does Catchtrial EDC+ offer? Catchtrial EDC+ provides Email/Help Desk, FAQ/Forum, Knowledge Base, Phone Support, and Chat. No reviewer feedback about support is available in the catalog data, so user experience with response times, helpfulness, or common frustrations cannot be summarized here. ## Features AI summary Based on 355 Clinical Trial Management reviews Capterra reviewers point to these as the top priorities when selecting clinical trial management software: - **21 CFR Part 11 Compliance** (**72%** of reviewers rated this feature as critical) - **HIPAA Compliant** (**76%**) - **Electronic Data Capture** (**51%**) Catchtrial EDC+ supports all three features that reviewers rate most highly: **21 CFR Part 11 Compliance**, **HIPAA Compliant**, and **Electronic Data Capture**. Together, these capabilities help businesses maintain regulatory compliance, protect sensitive patient information, and collect study data accurately, allowing teams to manage clinical trials with greater confidence and control. 21 CFR Part 11 Compliance Shows that electronic documents are authentic and linked to specific records Audit Trail A record of all activities within the system, including user access, changes made, etc. Clinical Study Management Tools to manage single or multiple clinical studies within a centralized platform Data Capture and Transfer Import, collect, and capture data from multiple sources Data Import/Export Import and export data to and from software applications Data Storage Management Manage and store data in a database Catchtrial EDC+ 20 features ### All Features - 21 CFR Part 11 Compliance: Shows that electronic documents are authentic and linked to specific records - Audit Trail: A record of all activities within the system, including user access, changes made, etc. - Clinical Study Management: Tools to manage single or multiple clinical studies within a centralized platform - Data Capture and Transfer: Import, collect, and capture data from multiple sources - Data Import/Export: Import and export data to and from software applications - Data Storage Management: Manage and store data in a database - Data Verification: Process of checking different types of data for accuracy to avoid errors or inconsistencies - Document Management: Store, manage, and track all electronic documents in a centralized location - Electronic Data Capture: Import, collect, and capture data from multiple sources - EMR/EHR: Create and securely store digital patient records - Financial Management: Plan, manage, and track the financial activities of an individual or organization - HIPAA Compliant: Compliant with HIPAA, which sets standards for sensitive patient data protection - Inventory Management: Track and manage inventory levels to maintain proper supply - Monitoring: Observe and track the demand, usage, progress or quality of a system, product, or user - Patient Management: Managing and tracking patient health, progress, communication, and treatment plans - Patient Monitoring: Observing and tracking a patient's health status, condition, and wellbeing - Patient Recruiting: Helps clinical trials/labs get patients for participation. - Randomization: Randomize the displayed order of questions and answer options - Scheduling: Plan availability and assign specific time slots for tasks and resources - Workflow Management: Create, design and manage workflows for repetitive tasks --- Features 4.0 (1) 4.0 Based on 1 reviews ## Pricing Value for money 4.0 (1) Value for money 4.0 (1) 4.0 Based on 1 reviews ## Support, customer service and training options Customer Service 4.0 (1) Support - Email/Help Desk - FAQs/Forum - Knowledge Base - Phone Support - 24/7 (Live rep) - Chat Training - In Person - Live Online - Webinars - Documentation - Videos Deployment - Web - Android - iPhone/iPad Typical users - Freelancers - Small businesses - Mid size businesses - Enterprises Customer Service 4.0 (1) 4.0 Based on 1 reviews ## User reviews Overall rating 5.0 Based on 1 reviews Filter by rating 5(1) 4(0) 3(0) 2(0) 1(0) Mentioned topic Sorted by most recent DM Donna M. CRA Medical Devices ### "Experience review of Catchtrial" 5.0 Overall Rating 5.0 5.0 Ease of Use 4.0 4.0 Features 4.0 4.0 Customer Service 4.0 4.0 Likelihood to Recommend 9/10 August 16, 2018 Very clean and easy to adapt; HelpDesk very thorough; always a Project Manager assigned. The ability to introduce newer modules during the course of the study depending on your needs is extremely helpful and financially a big plus! Pros Catchtrial can be purchased in a variety of platforms to incorporate as many modular capabilities as you prefer. From the simplest of do-it-yourself programming for smaller studies all through major full-blown studies requiring the expertise of event adjudicating and specific report-building. The software is clearly intuitive with tree-decision navigation and an in-depth knowledge base with tutorial. Cons Publishing into new versions of eCRFs is a bit involved; but the careful time taken to ensure you are doing the right thing is more important than the speed for transitioning. Review source Non-incentivized review: any software user can leave a review for any product listed on our site. All submitted reviews are subject to our verification process prior to publication. ## Top-rated software of 2026 ### Fill out the form and we'll send a list of the top-rated software based on real user reviews directly to your inbox.