# Best Clinical Trial Management Systems - Page 4 *By [Emma Stein](https://research.g2.com/insights/author/emma-stein)* Clinical trial management systems, also known as CTMS, clinical trial software, or clinical trial management software, manages the operations, processes, and data involved in clinical studies and trials. A CTMS centralizes all trial and study data, standardizes and streamlines workflows, and tracks and optimizes site, participant, investigator, and trial processes. Pharmaceutical companies, medical research institutes, and research centers managed by hospitals utilize clinical trial management software. This type of software is used by CROs, medical researchers, and trial administrators or sponsors to plan, manage, and monitor the entire lifecycle of clinical trials. All CTMS are designed to adhere to industry regulations so that trials can maintain compliance according to both institution and industry. To qualify for inclusion in the Clinical Trial Management (CTMS) category, a product must: - Find and manage participants for clinical trials - Plan and track clinical trial projects, including milestones and deadlines - Capture and analyze clinical trial information - Ensure regulatory compliance with laws protecting the privacy and the health of the participants ## G2 Grid® for Clinical Trial Management Systems ![G2 Grid® for Clinical Trial Management Systems plotting products by satisfaction and market presence](https://www.g2.com/categories/clinical-trial-management-systems/grids.png?focus%5B%5D=94249&focus%5B%5D=134478&focus%5B%5D=12463&focus%5B%5D=105941&focus%5B%5D=12354&focus%5B%5D=44665&focus%5B%5D=1191388&focus%5B%5D=1308616) Highlighted products: Viedoc, Clinical Research Suite, OnCore CTMS, Florence eBinders, Rave CTMS, Clario CTMS, Vial EDC + eSource, and TrialHub. Underlying data: [Grid® JSON](https://www.g2.com/categories/clinical-trial-management-systems/grids.json?focus%5B%5D=viedoc&focus%5B%5D=clinical-research-suite&focus%5B%5D=oncore-ctms&focus%5B%5D=florence-healthcare-florence-ebinders&focus%5B%5D=rave-ctms&focus%5B%5D=clario-ctms&focus%5B%5D=vial-edc-esource&focus%5B%5D=trialhub) ## How Many Clinical Trial Management Systems Products Does G2 Track? **Total Products under this Category:** 100 ### Category Stats (Jul 2026) - **Average Rating**: 4.2/5 The average rating of products in this category, based on all submitted ratings *Last updated: July 11, 2026* ## How Does G2 Rank Clinical Trial Management Systems Products? **Why You Can Trust G2's Software Rankings:** - 30 Analysts and Data Experts - 800+ Authentic Reviews - 100+ Products - Unbiased 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. ## Which Clinical Trial Management Systems Is Best for Your Use Case? - **Leader:** [Viedoc](https://www.g2.com/products/viedoc/reviews) - **Highest Performer:** [Clinical Research Suite](https://www.g2.com/products/clinical-research-suite/reviews) - **Easiest to Use:** [Viedoc](https://www.g2.com/products/viedoc/reviews) - **Top Trending:** [Clario CTMS](https://www.g2.com/products/clario-ctms/reviews) - **Best Free Software:** [Clinical Research Suite](https://www.g2.com/products/clinical-research-suite/reviews) --- **Sponsored** ### REDCap Cloud EDC REDCap Cloud offers a unified clinical research platform that brings together EDC, Randomization, ePRO and eConsent into a continuous data ecosystem, enabling real-time intelligence across the full lifecycle of IIT/IIS, RCT and RWE studies. Designed to support global Clinical Research for MedTech, Academic / IIS/ IIT, Biotech, Health Systems, Registries and RWE projects. [Visit website](https://www.g2.com/external_clickthroughs/record?secure%5Bad_program%5D=ppc&secure%5Bad_slot%5D=category_product_list&secure%5Bcategory_id%5D=446&secure%5Bchosen_at%5D=2026-07-13T05%3A30%3A34Z&secure%5Bdisplayable_resource_id%5D=1733&secure%5Bdisplayable_resource_type%5D=Category&secure%5Bmedium%5D=sponsored&secure%5Bplacement_reason%5D=neighbor_category&secure%5Bplacement_resource_ids%5D%5B%5D=1733&secure%5Bprioritized%5D=false&secure%5Bproduct_id%5D=1870742&secure%5Bresource_id%5D=446&secure%5Bresource_type%5D=Category&secure%5Bsource_type%5D=category_page&secure%5Bsource_url%5D=https%3A%2F%2Fwww.g2.com%2Fcategories%2Fclinical-trial-management-systems&secure%5Btoken%5D=85c0d057b9be6f888d02ac4ba6de5e9461c9be5fdca3b37b6b801414a674d76c&secure%5Burl%5D=https%3A%2F%2Fwww.redcapcloud.com%2F%3Futm_source%3Dg2%26utm_medium%3Dpaid%26utm_campaign%3Dg2-sponsored-edcm%26utm_content%3Dcategory-listing&secure%5Burl_type%5D=custom_url) --- ## What Are the Top-Rated Clinical Trial Management Systems Products in 2026? ### 1. [Monsana Assist](https://www.g2.com/products/monsana-assist/reviews) Patient pre-screening AI assistant for clinical trial recruitment. **Who Is the Company Behind Monsana Assist?** - **Seller:** [Monsana](https://www.g2.com/sellers/monsana) - **Year Founded:** 2024 - **HQ Location:** Rapertingenstraat, 3500, Hasselt, BE - **LinkedIn® Page:** https://www.linkedin.com/company/monsana-ai/ (3 employees on LinkedIn®) ### 2. [MyDataHelps](https://www.g2.com/products/mydatahelps/reviews) An innovative, no-code platform for conducting participant-centric digital clinical trials in record time. Collect eConsent, ePROs, and wearable device data from Fitbit, Garmin, Oura, Apple Watch, Google Fit and more. Connect to EHR and claims records for a more robust longitudinal record of each participant. All data is stored in the HIPAA-compliant, Meaningful Use Certified EDC HIEBus™ platform, and is then exported to researchers in an easy-to-use format, allowing scientists to focus on science. **Who Is the Company Behind MyDataHelps?** - **Seller:** [CareEvolution](https://www.g2.com/sellers/careevolution) - **Year Founded:** 2004 - **HQ Location:** Ann Arbor, US - **LinkedIn® Page:** http://www.linkedin.com/company/careevolution-inc (80 employees on LinkedIn®) ### 3. [oomnia](https://www.g2.com/products/oomnia/reviews) oomnia is a real-time SaaS platform that unifies all essential clinical trial tools-EDC, RTSM, CTMS, eTMF, eCOA, ePRO, and eConsent-into one cohesive system. With single sign-on, users save up to 75% of time spent navigating between systems. Its multi-tenant design allows stakeholders to manage multiple trials on a single instance and gain oversight of entire portfolios. No coding is required due to intuitive drag-and-drop features. oomnia is fully interoperable, eliminating integration issues, and offers role-based access with a user-friendly interface customizable by language and notifications. Real-time reporting, seamless randomization, and complete audit logs enhance efficiency and data accuracy. The platform complies with 21 CFR Part 11, EU Annex 11, and CDISC standards. ISO 27001 and ISO 9001 certified and FDA/Swissmedic inspected, oomnia enables up to 50% time and cost savings through streamlined, intelligent trial management. **Who Is the Company Behind oomnia?** - **Seller:** [Wemedoo AG](https://www.g2.com/sellers/wemedoo-ag) - **Year Founded:** 2020 - **HQ Location:** Steinhausen, CH - **LinkedIn® Page:** https://www.linkedin.com/company/wemedoo/ (37 employees on LinkedIn®) - **Phone:** +41 41 740 0124 ### 4. [OPRA Central Monitoring](https://www.g2.com/products/opra-central-monitoring/reviews) Centralized Monitoring Built for Modern Clinical Trials Improve trial performance by up to 30% with monitoring that reduces complexity and keeps your study on track. Focus on what matters most • Vizualize changes over time instantly • Quickly identify critical risks by uncovering hidden insights • Minimize wasted effort by directing attention where it’s needed Confidence in every decision • Full visibility with intelligent, dynamic data structures • Adapt easily to emerging needs and regulatory expectations • Demonstrate compliance with a clear evidence trail Efficiency across the board • Repetitive monitoring tasks are automated • Periodic review cycles are streamlined • Free up time and resources to concentrate on high-value activities **Who Is the Company Behind OPRA Central Monitoring?** - **Seller:** [Triumph Research Intelligence](https://www.g2.com/sellers/triumph-research-intelligence) - **Year Founded:** 2013 - **HQ Location:** Cambridge, GB - **LinkedIn® Page:** https://www.linkedin.com/company/tri-the-rbqm-experts (98 employees on LinkedIn®) ### 5. [Protocol Manager](https://www.g2.com/products/atlant-systems-protocol-manager/reviews) Protocol Manager helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development. **Who Is the Company Behind Protocol Manager?** - **Seller:** [Atlant Systems](https://www.g2.com/sellers/atlant-systems-ed8c181f-8e3d-4ab1-90b8-2902bd9ce3cf) - **HQ Location:** N/A - **LinkedIn® Page:** https://www.linkedin.com/company/llc-atlant-systems/ (2 employees on LinkedIn®) ### 6. [RealTime-Devana](https://www.g2.com/products/realtime-devana/reviews) RealTime-Devana is a holistic business intelligence platform designed specifically for research site organizations, driving transparency and accountability across all functional groups. From pipeline management and streamlined study start-up through to historical trial metrics, Devana provides one source of truth for all your clinical trial data and processes. Improve turnaround times and stand out to CROs and sponsors with Devana’s powerful workflow improvements and data analytics. **Who Is the Company Behind RealTime-Devana?** - **Seller:** [RealTime-CTMS](https://www.g2.com/sellers/realtime-ctms) - **Year Founded:** 2011 - **HQ Location:** San Antonio, US - **LinkedIn® Page:** https://www.linkedin.com/company/realtime-ctms-software-solutions (96 employees on LinkedIn®) ### 7. [Scienta Lab](https://www.g2.com/products/scienta-lab/reviews) Scienta Lab is an AI-powered platform pioneering Precision Immunology **Who Is the Company Behind Scienta Lab?** - **Seller:** [Scienta Lab](https://www.g2.com/sellers/scienta-lab) - **Year Founded:** 2021 - **HQ Location:** Paris, FR - **LinkedIn® Page:** https://www.linkedin.com/company/scienta-lab/ (19 employees on LinkedIn®) ### 8. [SimpleCTMS](https://www.g2.com/products/simplectms/reviews) SimpleTrials is a Clinical Trial Management System for Sponsors, CROs and Sites. SimpleCTMS was designed and developed to offer the benefits of a CTMS (Clinical Trial Management System) without the extensive upfront financial and resource commitments associated with traditional enterprise systems or the inherent inefficiencies of worksheet trackers. **Who Is the Company Behind SimpleCTMS?** - **Seller:** [Trial by Fire](https://www.g2.com/sellers/trial-by-fire) - **HQ Location:** N/A - **LinkedIn® Page:** https://www.linkedin.com/company/No-Linkedin-Presence-Added-Intentionally-By-DataOps (1 employees on LinkedIn®) ### 9. [SimpleTrials CTMS](https://www.g2.com/products/simpletrials-ctms/reviews) SimpleTrials is the industry’s first on-demand, subscription-based CTMS for sites, vendors and sponsors. SimpleTrials CTMS provides the robust functionality needed to manage the most complex studies with the ease of use that busy teams require. **Who Is the Company Behind SimpleTrials CTMS?** - **Seller:** [TrialStat](https://www.g2.com/sellers/trialstat) - **Year Founded:** 2003 - **HQ Location:** Montreal, CA - **LinkedIn® Page:** https://www.linkedin.com/company/trialstat/ (12 employees on LinkedIn®) ### 10. [Smart Omix](https://www.g2.com/products/smart-omix/reviews) Smart Omix by Sharecare is a software platform enabling researchers to design, launch, manage, and analyze real-world digital clinical studies at scale. Researchers across the healthcare and life sciences industry can leverage our self-service platform or concierge study- building services to conduct rigorous, high- quality, real-world data collection via the Smart Omix app (available on iOS and Android). Using our first-of-its-kind SaaS model, researchers can include rich data into studies to gain a sharper view of the real lived experiences of study participants—, from photo, video and audio ePROs, to pre-integrated modules for patient-generated health data across popular wearables and devices today. Participant-centricity is core to how we have designed our platform. From adherence-based compensation modules to AI ePROs like a ‘smart selfie’ to ingest body mass index (BMI) information, or ‘smart medication’ to allow for an immediate photo-to-drug-description for participants, participants are first-class citizens and users of our platform. Our team is on a mission to democratize real-world clinical research by creating software that is technologically, economically, and socially accessible for the next generation of real-world data collection. Visit www.sharecare.com/smartomix to learn more about how our platform can facilitate your next decentralized clinical trial, virtual clinical trial, or real-world evidence generation study. **Who Is the Company Behind Smart Omix?** - **Seller:** [Sharecare](https://www.g2.com/sellers/sharecare) - **Year Founded:** 2010 - **HQ Location:** Atlanta, Georgia, United States - **LinkedIn® Page:** https://www.linkedin.com/company/sharecare-inc (3,821 employees on LinkedIn®) ### 11. [Studylog](https://www.g2.com/products/studylog/reviews) Studylog is in-vivo study management software used by pharmaceutical companies, biotech firms, contract research organizations (CROs), and academic research institutions to manage the workflow of in-vivo research studies. The platform covers the study lifecycle from design through reporting, including study design and scheduling, task and measurement tracking, data acquisition, randomization, data analysis, and report generation. The software is used to replace spreadsheet-based tracking methods with a centralized database that stores study data, protocols, and results in a single system. Data can be entered manually or collected automatically through integrations with wired and wireless scales, calipers, and blood analyzers. Studylog also integrates with GraphPad Prism for graphing and statistical analysis, and supports bioluminescence imaging (BLI) data. Key functionality includes: - Study design tools, including reusable study templates and the ability to clone prior studies for follow-up research - Task and measurement scheduling with timers and completion tracking - Multiple randomization methods (stratified, matched distribution, multi-parameter, and pure random), with options to randomize by parameters such as age, body weight, or tumor volume - Automated data collection from connected laboratory devices - Built-in graphing, including box plots, group mean line graphs, and Kaplan-Meier survival curves - A calendar view for scheduling and tracking tasks across multiple concurrent studies - Standardized dictionaries and nomenclature for consistent data entry across studies - Access controls and permissions by user, team, and study - A web API for integration with electronic lab notebooks (ELNs) and other systems Studylog is offered as a desktop application and includes offline access, allowing users to continue working with synchronized study data when network connectivity is unavailable. The company has provided in-vivo study management software for more than 20 years and offers customer support staffed by former in-vivo researchers. **Who Is the Company Behind Studylog?** - **Seller:** [Studylog Systems](https://www.g2.com/sellers/studylog-systems) - **Year Founded:** 2003 - **HQ Location:** Pacifica, US - **LinkedIn® Page:** https://www.linkedin.com/company/studylog-systems-inc (18 employees on LinkedIn®) ### 12. [Studypages](https://www.g2.com/products/studypages/reviews) Clinical trial management system **Who Is the Company Behind Studypages?** - **Seller:** [teamscope](https://www.g2.com/sellers/teamscope) - **Year Founded:** 2014 - **HQ Location:** SF Bay Area, US - **Twitter:** @TeamscopeApp (2,092 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/studypages-platform/ (11 employees on LinkedIn®) ### 13. [SUMMA Real-World Evidence (RWE) Platform](https://www.g2.com/products/summa-real-world-evidence-rwe-platform/reviews) SUMMA™ is a configurable solution that allows researchers to generate new insights by integrating large disparate real-world data sources such as electronic health records (EHR), historical clinical trails data, EDC, eCOA, ePRO’s, claims data, disease registries, labs, medical devices, wearables, and Health IOT. **Who Is the Company Behind SUMMA Real-World Evidence (RWE) Platform?** - **Seller:** [Precision Digital Health](https://www.g2.com/sellers/precision-digital-health) - **Year Founded:** 2015 - **HQ Location:** Irvine, US - **Twitter:** @PrecisionDH (1,462 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/precision-digital-health-inc (24 employees on LinkedIn®) ### 14. [SyMetric](https://www.g2.com/products/symetric/reviews) SyMetric offers cloud-based, end-to-end solutions for Clinical Research, from Manufacturing to the Submissions. The Product suit is built as an ERP, on a single database providing a seamless flow of data across modules. Products: 1. SyMetric Clinical Trial Platform SyMetric Integrated Cloud-Based Clinical Trial Platform is fully modularized, allowing you to choose the right solution that can be configured to suit your trial requirements. You can plan, monitor, and manage trials effectively, every step of the way. Designed, developed, and deployed by us, our all-encompassing set of solutions that is IRT/IWRS, EDC, Medical Coding, CTM, and Trial Analytics on a single database built to work seamlessly with your existing ecosystem and processes. It covers various processes in Clinical Trials – including Study Master Management, Subject Management, Clinical Supplies Management, Data Management, and Medical Coding. With SyMetric Clinical Trial Platform, you can manage, monitor, analyze, and report with ease by configuring the solutions to your specific needs – whether you are a Pharmaceutical Sponsor, Clinical Research Organization (CRO), or from the Academia. 2. SyMetric Trial Analytics The SyMetric Trial Analytics solution helps you make informed decisions while planning a new Clinical Trial using insights from historic study data and performance analytics of stakeholders such as CROs, Investigation Sites, and Investigators. With our Analytics Tool, you can cut Trial Planning time significantly and enhance efficiency. Also, the system is built on the SAP Business Technology Platform, enabling you to explore various services that SAP has to offer in the Cloud. Our solution can be integrated with your system to deliver insightful analysis while leveraging cloud initiatives from SAP in Life Sciences. Here are the various sources of data that we analyze to help you plan effectively. **Average Rating:** 5.0/5.0 **Total Reviews:** 1 **Who Is the Company Behind SyMetric?** - **Seller:** [SyMetric Systems](https://www.g2.com/sellers/symetric-systems) - **Year Founded:** 2012 - **HQ Location:** Bengaluru, IN - **LinkedIn® Page:** https://www.linkedin.com/company/symetric-systems/ (38 employees on LinkedIn®) **Who Uses This Product?** - **Company Size:** 100% Enterprise #### What Are Recent G2 Reviews of SyMetric? **"[It is a a experience as I have been getting hang things](https://www.g2.com/survey_responses/symetric-review-7147186)"** **Rating:** 5.0/5.0 stars *— Thando M.* [Read full review](https://www.g2.com/survey_responses/symetric-review-7147186) --- ### 15. [Syncora](https://www.g2.com/products/syncora/reviews) Syncora is a cloud-based platform revolutionizing study startups for CROs, sponsors, and investigative sites. Born from relentless innovation, it automates workflows, captures and displays real-time data, and empowers teams to navigate complex startup processes with speed and precision. With a user-friendly interface, secure cloud backup, and a commitment to transparency, Syncora ensures timelines are met, delays are addressed proactively, and clinical trial operations run seamlessly from day one. 🌐Learn more: www.syncora.com **Who Is the Company Behind Syncora?** - **Seller:** [Digital Auxilius](https://www.g2.com/sellers/digital-auxilius-1ffc5371-cd5f-4318-a8b9-4654781d8122) - **Year Founded:** 2016 - **HQ Location:** Farmington Hills, US - **LinkedIn® Page:** http://www.linkedin.com/company/digital-auxilius (72 employees on LinkedIn®) ### 16. [ThoughtSphere](https://www.g2.com/products/thoughtsphere/reviews) ThoughtSphere’s mission is to help life science companies develop and deliver treatments to patients faster and smarter using data science. With our innovative platform, biopharma, medical device sponsors and CROs not only can reduce and optimize clinical development costs but also enhance efficiency and effectiveness in the clinical trial processes, and gain near real-time actionable insights. Founded by clinical information and technology industry experts, ThoughtSphere aims to deliver on the promise of big data to drive health innovation. Our product suite includes ClinHUB – the source-system agnostic data lake and integration platform that bridges the gap from data transformation to analytics, ClinACT – the interactive visualization and analytics platform that enables RBM, QM and CRO Oversight and SPACE – the integrated site budgeting, payments and contracting solution. **Who Is the Company Behind ThoughtSphere?** - **Seller:** [ThoughtSphere](https://www.g2.com/sellers/thoughtsphere) - **Year Founded:** 2015 - **HQ Location:** San Jose, US - **LinkedIn® Page:** https://www.linkedin.com/company/thoughtsphere-inc (33 employees on LinkedIn®) ### 17. [Trialflare](https://www.g2.com/products/trialflare/reviews) Trialflare is the flexible platform for getting accurate research data. Trialflare is a platform that allows researchers and people involved in R&D activity to collect meaningful data from participants as part of a controlled trial or survey. It is used across the cosmetics, health, and supplements space to help organisations understand the effect of a product or development. Whilst being a security-focused product, Trialflare is also easy to use for researchers and participants alike, with our web applications and native mobile apps. **Who Is the Company Behind Trialflare?** - **Seller:** [Seastorm Limited](https://www.g2.com/sellers/seastorm-limited) - **Year Founded:** 2018 - **HQ Location:** Cardiff, GB - **LinkedIn® Page:** https://www.linkedin.com/company/trialflare (1 employees on LinkedIn®) ### 18. [Trially AI Clinical Trial Recruitment](https://www.g2.com/products/trially-ai-clinical-trial-recruitment/reviews) Trially is the first AI-native clinical trial platform that matches, engages and enrolls patients at breakthrough speed and ~95% accuracy. Loved by customers, Trially LLM agents fill trials faster—with 2-6x increase in enrollment rate, 73% fewer screen fails, and 91% less prescreening time. Trially’s IRB-approved agents rapidly prescreen patients from any clinical data source, fully compliant with HIPAA, SOC 2, FDA 21 CFR Part 11, and ISO 27001. Designed to meet the needs of Physicians, Sites, Sponsors and CROs, Trially AI empowers you to achieve outstanding results in clinical research. **Who Is the Company Behind Trially AI Clinical Trial Recruitment?** - **Seller:** [Trially](https://www.g2.com/sellers/trially) - **Year Founded:** 2023 - **HQ Location:** Kansas City, US - **LinkedIn® Page:** https://www.linkedin.com/company/trially/ (12 employees on LinkedIn®) ### 19. [TrialPro](https://www.g2.com/products/trialpro/reviews) UpSite Clinical offers TrialPro, an AI-enabled clinical trial budgeting software designed to assist research sites, sponsors and CROs in creating and negotiating study budgets and Medicare coverage analysis. The tool uses Fair Market Value benchmarks and automates various budgeting processes to ensure that sites avoid unpaid work and save time. Built by industry veterans, TrialPro analyzes protocols and generates budget grids while identifying unbudgeted work and generating coverage analysis. Their services cater to clinical research sites, sponsors and CROs seeking efficient and effective budget management solutions. **Who Is the Company Behind TrialPro?** - **Seller:** [Upsite Clinical](https://www.g2.com/sellers/upsite-clinical) - **Year Founded:** 2023 - **HQ Location:** N/A - **LinkedIn® Page:** https://www.linkedin.com/company/upsite-clinical/ (11 employees on LinkedIn®) ### 20. [Trialytix](https://www.g2.com/products/trialytix/reviews) Trialytix is the first software solution that covers all essential budget and cost operations of your clinical trial project. **Who Is the Company Behind Trialytix?** - **Seller:** [Trialytix](https://www.g2.com/sellers/trialytix) - **Year Founded:** 2023 - **HQ Location:** Fulda, DE - **LinkedIn® Page:** https://www.linkedin.com/company/trialytix-io/ (3 employees on LinkedIn®) ### 21. [Veeva CTMS](https://www.g2.com/products/veeva-ctms/reviews) With a real-time view across clinical trial processes, Vault CTMS improves operational efficiency, streamlines collaboration, and enables faster, higher-quality trial execution. **Who Is the Company Behind Veeva CTMS?** - **Seller:** [Veeva](https://www.g2.com/sellers/veeva) - **Year Founded:** 2007 - **HQ Location:** Pleasanton, CA - **Twitter:** @veevasystems (6,133 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/402048/ (9,958 employees on LinkedIn®) - **Ownership:** NYSE: VEEV ### 22. [Velos eResearch](https://www.g2.com/products/velos-eresearch/reviews) WCG Velos is a Clinical Research Management Solution (CRMS) designed to automate and centralize financial, operational, and administrative research activities. Leading research institutions, sites, and networks use the system’s integrated technology to consolidate and scale their research program, increasing profit, and improving protocol and regulatory compliance **Who Is the Company Behind Velos eResearch?** - **Seller:** [Velos](https://www.g2.com/sellers/velos) - **HQ Location:** Cary, US - **LinkedIn® Page:** https://www.linkedin.com/company/wirb-copernicus-group/ (1,332 employees on LinkedIn®) ### 23. [Your Research CTMS](https://www.g2.com/products/your-research-ctms/reviews) Your Research is a leading Clinical Trial Management Software development company whose mission is to make a positive impact on people’s lives by advancing research processes that improve health outcomes. Your Research achieves this by offering the research industry a full suite of flexible, scalable, and integrable online modules derived from researcher led feedback. Your Research Clinical Trial Management System (CTMS) is tailored to streamline trials, prioritising patient-centricity and process efficiency. Key features include protocol-driven automation for time-saving and accurate data input. Patient experiences are enhanced through digitalisation, optimising in-person tasks, visit bookings, and eConsent with a focus on improving retention. Predict future events by tracking historical metrics. Access user-friendly 'pay per play' eCOA modules, such as ePRO, eConsent, and eCRF, to elevate trial efficiency. Your Research CTMS is a comprehensive integrable solution, ensuring a seamless and patient-focused research experience and is compliant with and or adheres to the following best practices: - HIPAA - 21 CFR Part 11 - Good Clinical Practice (GCP) - ISO 27001 - GDPR - FDA 21 CFR Part 50 - FDA 21 CFR Part 54 - ICH E6 (R2 **Who Is the Company Behind Your Research CTMS?** - **Seller:** [Your Research](https://www.g2.com/sellers/your-research) - **Year Founded:** 2019 - **HQ Location:** Amsterdam , NL - **LinkedIn® Page:** https://www.linkedin.com/company/your-research/ (8 employees on LinkedIn®) ### 24. [Zelthy-Clinical Trial Transparency](https://www.g2.com/products/zelthy-clinical-trial-transparency/reviews) What is this product? Zelthy Clinical Trial Transparency is an application for pharmaceutical regulatory and compliance teams managing clinical trial disclosure obligations. It tracks submission deadlines across registries (ClinicalTrials.gov, EU CTR, and others), manages the preparation and filing of registry submissions and results postings, and performs cross-registry consistency checks to ensure disclosures align across platforms. Key Features & Functionalities - Deadline tracking across multiple clinical trial registries - Submission preparation and filing workflows - Results posting management with milestone tracking - Cross-registry consistency checks - Compliance calendar with automated reminders Primary Solution & Value Clinical trial transparency requirements have expanded significantly — FDAAA, EU CTR, and other regulations mandate timely registration and results posting with specific deadlines. Missed deadlines result in regulatory citations and reputational damage. This application tracks disclosure obligations across registries and automates deadline management, ensuring trials meet transparency requirements on schedule. **Who Is the Company Behind Zelthy-Clinical Trial Transparency?** - **Seller:** [Healthlane Technologies](https://www.g2.com/sellers/healthlane-technologies) - **Year Founded:** 2017 - **HQ Location:** Seattle, US - **LinkedIn® Page:** https://www.linkedin.com/company/zelthy1 (33 employees on LinkedIn®) ### 25. [Zelthy-Compassionate Access](https://www.g2.com/products/zelthy-compassionate-access/reviews) What is this product? Zelthy Compassionate Access is an application for pharmaceutical companies managing expanded access (compassionate use) programs. It handles the complete program workflow: patient request intake, physician and medical review, ethics committee approval, regulatory filing (FDA, TGA, EMA), and logistics coordination for drug supply — replacing the manual, multi-step approval process that often delays patient access to investigational therapies. Key Features & Functionalities - Patient request intake with physician documentation - Medical review and clinical assessment workflows - Ethics committee approval management - Regulatory filing for FDA, TGA, EMA, and other authorities - Drug supply logistics coordination - Program analytics and reporting Primary Solution & Value Expanded access programs involve a complex multi-step approval chain — medical review, ethics approval, regulatory filing — that can delay patient access to investigational therapies by weeks. This application digitizes the full approval workflow, reducing cycle time while maintaining the documentation required for regulatory compliance. **Who Is the Company Behind Zelthy-Compassionate Access?** - **Seller:** [Healthlane Technologies](https://www.g2.com/sellers/healthlane-technologies) - **Year Founded:** 2017 - **HQ Location:** Seattle, US - **LinkedIn® Page:** https://www.linkedin.com/company/zelthy1 (33 employees on LinkedIn®) ## What Is Clinical Trial Management Systems? [Clinical Research Software](https://www.g2.com/categories/clinical-research) ## What Software Categories Are Similar to Clinical Trial Management Systems? - [Electronic Data Capture (EDC) Software](https://www.g2.com/categories/electronic-data-capture-edc)