# Best Clinical Trial Management Systems - Page 7

## How Many Clinical Trial Management Systems Products Does G2 Track?

**Total Products under this Category:** 102

### Category Stats (Jul 2026)

- **Average Rating:** 4.22/5 (↑0.02 vs Jun 2026) The average rating of products in this category, based on all submitted ratings

_Last updated: July 31, 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
- 102+ 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.

## 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=12463&focus%5B%5D=94249&focus%5B%5D=134478&focus%5B%5D=105941&focus%5B%5D=12354&focus%5B%5D=44665&focus%5B%5D=1191388&focus%5B%5D=1308616)

Highlighted products: OnCore CTMS, Viedoc, Clinical Research Suite, 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=oncore-ctms&focus%5B%5D=viedoc&focus%5B%5D=clinical-research-suite&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)

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=5979278d3ae387fbf496ee4e612a22163cfa7ca6961fd62aafd22f938af2798a&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fsymetric-systems%2F&secure%5Burl_type%5D=linkedin_company_website)  
38 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 100% Large

#### 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)

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=05cde7e37177941551b89a3444eda4923fa69a602250b616aa0b6ea0c666fef0&secure%5Burl%5D=http%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fdigital-auxilius&secure%5Burl_type%5D=linkedin_company_website)  
72 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=6cf04337b715b9a559d636ebc72565ca56650cc3d7b2da76fa292f2f9e286c9c&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fthoughtsphere-inc&secure%5Burl_type%5D=linkedin_company_website)  
33 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=fef3b61c2f9a2429298003fe67004cbfd29e7d328917d7aec6b482ec66ce0860&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Ftrialflare&secure%5Burl_type%5D=linkedin_company_website)  
1 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=8cbeea9bd41d5cc1121ecee56414d5e2757f6074920a50e1e7e37296291afa3a&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Ftrially%2F&secure%5Burl_type%5D=linkedin_company_website)  
12 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=ffa10e0e0a473ec372162caa8adb0b312562e812cdc00027aa63413df18f38a1&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fupsite-clinical%2F&secure%5Burl_type%5D=linkedin_company_website)  
11 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=4255b05278752ffd0ad3e0747cd45f089845f0ac2d3b549672c79c5110c93af2&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Ftrialytix-io%2F&secure%5Burl_type%5D=linkedin_company_website)  
3 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=09d1882ac479495db33963e82af224cfab6bd595516d089eb06329a0022b3561&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F402048%2F&secure%5Burl_type%5D=linkedin_company_website)  
9,958 employees on LinkedIn®
- **Ownership:** NYSE: VEEV

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=82e049b02d76265fb87cdc7ac6aa67427b65599f8c673f408c2287e1f7d6eef2&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fwirb-copernicus-group%2F&secure%5Burl_type%5D=linkedin_company_website)  
1,332 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=0a7f835d45e58d8182aff0532e9a7a50295456074b957a3e0b5daca2e2d5586e&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fyour-research%2F&secure%5Burl_type%5D=linkedin_company_website)  
8 employees on LinkedIn®

### [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:** [Zelthy](https://www.g2.com/sellers/zelthy-2026-07-16)
- **Year Founded:** 2017
- **HQ Location:** Seattle, US
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=c2ee5c63810720eac3126d408f4ab408b1a0d6a37dc5d8220e1c3795c8dc9dfd&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fzelthy1&secure%5Burl_type%5D=linkedin_company_website)  
33 employees on LinkedIn®

### [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:** [Zelthy](https://www.g2.com/sellers/zelthy-2026-07-16)
- **Year Founded:** 2017
- **HQ Location:** Seattle, US
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=c2ee5c63810720eac3126d408f4ab408b1a0d6a37dc5d8220e1c3795c8dc9dfd&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fzelthy1&secure%5Burl_type%5D=linkedin_company_website)  
33 employees on LinkedIn®

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- [Electronic Data Capture (EDC)](/categories/electronic-data-capture-edc)

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[Browse Clinical Trial Management Systems Themes](/categories/clinical-trial-management-systems/themes)

 ![Emma Stein](/assets/transparent-ad5be28fbcd25b7b08d2cebe1d957125437fb5407d75ee717965ad22c8808791.gif "Emma Stein")
ES

Researched and written by [Emma Stein](https://research.g2.com/insights/author/emma-stein)

Updated October 3, 2024

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

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