Best Clinical Trial Management Systems

How Many Clinical Trial Management Systems Products Does G2 Track?

Total Products under this Category: 222

Category Stats (Nov 2026)

  • Average Rating: 4.27/5 (↑0.03 vs Oct 2026) The average rating of products in this category, based on all submitted ratings
  • Top Trending Product: TrialKit (+0.4%) - Among all products in this category, TrialKit recorded the largest rating increase compared to last month

Last updated: November 01, 2026

How Does G2 Rank Clinical Trial Management Systems Products?

Why You Can Trust G2's Software Rankings:

  • 30 Analysts and Data Experts
  • 900+ Authentic Reviews
  • 222+ Products
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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

Highlighted products: OnCore CTMS, Viedoc, Clinical Research Suite, Florence eBinders, Rave CTMS, Clario CTMS, Vial EDC + eSource, and TrialKit.

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=trialkit)

OnCore CTMS

OnCore CTMS is the trusted clinical trial management system (CTMS) used by nearly 90% of NCI-designated cancer centers and more than 90 of the top 125 academic medical centers. It streamlines operational, financial, and regulatory workflows to improve efficiency and quality across the research lifecycle. OnCore supports research sites and institutions with strong financial compliance through integrations with billing systems that enable end-to-end financial management. Deep EMR integrations provide seamless connectivity with widely used institutional systems. Additionally, advanced analytics deliver standardized, consistent reporting—including NCI reporting—offering clear visibility into a comprehensive set of metrics. OnCore also features exclusive, turnkey integrations with Advarra’s eReg and eSource systems, enhancing connectivity and driving greater efficiency across research workflows.

Average Rating: 4.4/5.0

Total Reviews: 14

How Do G2 Users Rate OnCore CTMS?

  • Data Centralization: 8.9/10 (Category avg: 8.7/10)
  • Quality of Support: 8.9/10 (Category avg: 8.6/10)
  • Documentation: 7.5/10 (Category avg: 8.4/10)
  • Site Management: 8.3/10 (Category avg: 8.6/10)

Who Is the Company Behind OnCore CTMS?

  • Seller: Advarra
  • Year Founded: 1983
  • HQ Location: Columbia, US
  • LinkedIn® Page: www.linkedin.com
    1,863 employees on LinkedIn®

Who Uses This Product?

  • Top Industries: Research
  • Company Size: 57% Large, 29% Medium

What Are Recent G2 Reviews of OnCore CTMS?

Viedoc

Viedoc streamlines clinical trials with a powerful, web-based eClinical suite centered around EDC. Designed for efficiency, compliance, and seamless collaboration, our feature-rich platform accelerates research and simplifies data collection, management, and analysis. Trusted in 75+ countries, Viedoc powers 7,000+ studies with more than 1.6M+ participants, bringing life-changing treatments to market faster.

Average Rating: 4.5/5.0

Total Reviews: 233

How Do G2 Users Rate Viedoc?

  • Data Centralization: 8.4/10 (Category avg: 8.7/10)
  • Quality of Support: 9.2/10 (Category avg: 8.6/10)
  • Documentation: 8.5/10 (Category avg: 8.4/10)
  • Site Management: 8.8/10 (Category avg: 8.6/10)

Who Is the Company Behind Viedoc?

  • Seller: Viedoc Technologies
  • Company Website:
  • Year Founded: 2003
  • HQ Location: Uppsala, Uppsala County
  • LinkedIn® Page: www.linkedin.com
    133 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Data Manager, Clinical Data Manager
  • Top Industries: Pharmaceuticals, Research
  • Company Size: 36% Large, 33% Small

What Do G2 Reviewers Say About Viedoc?

AI-generated summary from verified user reviews

Pros
  • Users value the user-friendly interface of Viedoc, enabling easy navigation and efficient data management.
  • Users value the user-friendly interface of Viedoc, enhancing navigation and efficiency for all clinical trial participants.
  • Users love Viedoc for its intuitive interface, which simplifies navigation and enhances overall efficiency in data management.
  • Users praise Viedoc's excellent customer support, noting the team's responsiveness and helpful training resources for quick adoption.
  • Users value Viedoc for its user-friendly design, enhancing efficiency and simplifying the clinical research process.
Cons
  • Users experience slow performance with Viedoc, especially when dealing with heavy forms or large data volumes.
  • Users find the advanced features complex, often needing extra training which delays overall adoption of Viedoc.
  • Users express frustration over limited access control, citing issues like single-user design access and automatic logouts.
  • Users find form design issues in Viedoc, including limitations on repeating fields and complex logic handling.
  • Users note the missing features in Viedoc, particularly the lack of bulk signatures and collaborative editing options.

What Are Recent G2 Reviews of Viedoc?

What Are G2 Users Discussing About Viedoc?

Clinical Research Suite

ABOUT ResearchManager is an all-in-one platform that makes clinical research smarter, faster, and more efficient. With the Clinical Research Suite, we provide a fully integrated solution for academic institutions, healthcare organizations, CROs, and sponsors across the entire clinical research lifecycle. From study setup and regulatory approval to recruitment, data capture, and monitoring. By centralizing processes and data on a single platform, ResearchManager reduces complexity, minimizes errors, and enhances compliance and collaboration. OUR MISSION Our mission is to digitalize, accelerate, and optimize research worldwide, enabling innovative treatments and scientific insights to reach patients sooner. We believe advancing healthcare starts with advancing research, and we empower organizations to make that happen. OUR PLATFORM - THE CLINICAL RESEARCH SUITE Clinical Data Management: Tools to recruit the right participants and efficiently capture, manage, and validate research data, reducing errors and saving time. • Electronic Data Capture (EDC) • Electronic Patient-Reported Outcomes (ePRO) • Randomization and Trial Supply Management (RTSM) • Electronic Informed Consent (eConsent) • Patient Recruitment Clinical Operations: Tools that centralize submissions, documentation, and workflows to streamline trial management and strengthen collaboration. These are all modular and fully configurable. • Clinical Trial Management System (CTMS) • Electronic Trial Master File (eTMF) • Regulatory Information Management System (RIMS) LEARN MORE • Request a FREE Demo:https://my researchmanager.com/en/request-inquiry/ • Get a Price Estimate in 1 Minute: https://my-researchmanager.com/en/pricing/

Average Rating: 3.8/5.0

Total Reviews: 205

How Do G2 Users Rate Clinical Research Suite?

  • Data Centralization: 7.4/10 (Category avg: 8.7/10)
  • Quality of Support: 7.6/10 (Category avg: 8.6/10)
  • Documentation: 7.5/10 (Category avg: 8.4/10)
  • Site Management: 7.2/10 (Category avg: 8.6/10)

Who Is the Company Behind Clinical Research Suite?

Who Uses This Product?

  • Who Uses This: PhD student, Researcher
  • Top Industries: Hospital & Health Care, Research
  • Company Size: 55% Large, 33% Small

What Do G2 Reviewers Say About Clinical Research Suite?

AI-generated summary from verified user reviews

Pros
  • Users find the ease of use of Clinical Research Suite beneficial, with a clear menu structure and self-explanatory features.
  • Users appreciate the interface clarity of Clinical Research Suite, finding it easy to navigate and organize tasks.
  • Users appreciate the user-friendly interface of the Clinical Research Suite, making it easy to navigate and use.
  • Users appreciate the user-friendly interface and comprehensive features of the Clinical Research Suite for efficient research management.
  • Users appreciate the easy workflow of Clinical Research Suite, effectively managing all aspects of their research.
Cons
  • Users struggle with poor navigation due to excessive clicking and unintuitive steps, making data access frustrating and time-consuming.
  • Users find the missing features in Clinical Research Suite frustrating, complicating tasks and hindering overall usability.
  • Users find a bit of a learning curve and navigation challenges, complicating their initial experience with the suite.
  • Users find the slow performance due to excessive clicks and tab navigation frustrating and time-consuming.
  • Users face data management issues due to unclear integration, confusing labels, and cumbersome data export processes.

What Are Recent G2 Reviews of Clinical Research Suite?

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Florence eBinders

Florence eBinders is a specialized electronic investigator site file (eISF) solution designed to enhance the efficiency and organization of clinical trial investigative sites. By transitioning from traditional paper-based processes to streamlined electronic workflows, Florence eBinders facilitates a more effective site experience, enabling remote monitoring, startup, and source data verification. This innovative platform is utilized by over 65,000 clinical trial sites, underscoring its significance in the research community. The primary target audience for Florence eBinders includes clinical research organizations, investigative sites, and sponsors involved in the management of clinical trials. These users benefit from a paper-free environment that not only simplifies research operations but also ensures adherence to stringent global compliance standards. Florence eBinders is particularly valuable for sites looking to reduce administrative burdens and enhance collaboration among stakeholders, including clinical trial monitors and regulatory bodies. Key features of Florence eBinders include advanced integrations that connect seamlessly with various site-based systems such as Clinical Trial Management Systems (CTMS), electronic consent (eConsent) platforms, and Institutional Review Board (IRB) portals. This integration capability minimizes repetitive tasks by allowing for the efficient sharing of documents and data across different platforms. As a result, users can focus more on critical research activities rather than getting bogged down by administrative overhead. Moreover, Florence eBinders is designed with user-friendliness in mind, making it accessible for a wide range of users, regardless of their technical expertise. The platform supports over 3 million research actions each month, demonstrating its robust functionality and reliability in managing clinical trial documentation. By providing a comprehensive site-based platform for electronic workflows, Florence eBinders not only enhances operational efficiency but also contributes to the overall success of clinical trials. In summary, Florence eBinders stands out in the realm of electronic investigator site file solutions by offering a complete, integrated, and user-friendly platform that addresses the unique challenges faced by clinical trial sites. Its ability to streamline processes, ensure compliance, and facilitate collaboration makes it an essential tool for those involved in clinical research.

Average Rating: 4.5/5.0

Total Reviews: 109

How Do G2 Users Rate Florence eBinders?

  • Data Centralization: 8.8/10 (Category avg: 8.7/10)
  • Quality of Support: 9.4/10 (Category avg: 8.6/10)
  • Documentation: 9.2/10 (Category avg: 8.4/10)
  • Site Management: 9.1/10 (Category avg: 8.6/10)

Who Is the Company Behind Florence eBinders?

Who Uses This Product?

  • Who Uses This: Clinical Research Coordinator
  • Top Industries: Research, Hospital & Health Care
  • Company Size: 38% Medium, 32% Small

What Are Recent G2 Reviews of Florence eBinders?

Rave CTMS

Medidata CTMS was created with powerful modules for outsourcing, site monitoring and site payments you can turn on together or separately as you need them.

Average Rating: 4.2/5.0

Total Reviews: 19

How Do G2 Users Rate Rave CTMS?

  • Data Centralization: 8.3/10 (Category avg: 8.7/10)
  • Quality of Support: 8.0/10 (Category avg: 8.6/10)
  • Documentation: 10.0/10 (Category avg: 8.4/10)
  • Site Management: 8.3/10 (Category avg: 8.6/10)

Who Is the Company Behind Rave CTMS?

  • Seller: Medidata
  • Year Founded: 1999
  • HQ Location: New York, NY
  • LinkedIn® Page: www.linkedin.com
    2,751 employees on LinkedIn®

Who Uses This Product?

  • Top Industries: Hospital & Health Care, Pharmaceuticals
  • Company Size: 48% Large, 35% Medium

What Are Recent G2 Reviews of Rave CTMS?

What Are G2 Users Discussing About Rave CTMS?

Clario CTMS

CTMS used to create a natural next step to bring Office tools, business process workflow, and documents into the regulated world.

Average Rating: 3.9/5.0

Total Reviews: 12

How Do G2 Users Rate Clario CTMS?

  • Data Centralization: 8.3/10 (Category avg: 8.7/10)
  • Quality of Support: 8.3/10 (Category avg: 8.6/10)
  • Documentation: 9.2/10 (Category avg: 8.4/10)
  • Site Management: 8.6/10 (Category avg: 8.6/10)

Who Is the Company Behind Clario CTMS?

  • Seller: Clario
  • Year Founded: 1972
  • HQ Location: Princeton, NJ
  • LinkedIn® Page: www.linkedin.com
    7,213 employees on LinkedIn®

Who Uses This Product?

  • Top Industries: Pharmaceuticals
  • Company Size: 50% Large, 33% Small

What Are Recent G2 Reviews of Clario CTMS?

What Are G2 Users Discussing About Clario CTMS?

Vial EDC + eSource

Discover Vial EDC, the cloud-native Electronic Data Capture (EDC) platform that combines exceptional performance with a user-friendly design for clinical research. Supercharged by Vial eSource, the Vial EDC is the core of Vial’s fully-compliant (21 CFR Part 11, HIPAA, GDPR) eClinical technology suite. Vial EDC simplifies clinical research data management through fast database builds, unlimited data integrations, and performance-boosting user features (end-to-end audit trails, comprehensive statuses, simple query and review management, etc).

Average Rating: 4.5/5.0

Total Reviews: 22

How Do G2 Users Rate Vial EDC + eSource?

  • Data Centralization: 9.8/10 (Category avg: 8.7/10)
  • Quality of Support: 9.5/10 (Category avg: 8.6/10)
  • Documentation: 9.7/10 (Category avg: 8.4/10)
  • Site Management: 10.0/10 (Category avg: 8.6/10)

Who Is the Company Behind Vial EDC + eSource?

  • Seller: Vial
  • Year Founded: 2020
  • HQ Location: San Francisco, California
  • LinkedIn® Page: www.linkedin.com
    158 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Clinical Research Coordinator
  • Top Industries: Research
  • Company Size: 64% Small, 41% Medium

What Are Recent G2 Reviews of Vial EDC + eSource?

TrialKit

TrialKit is a unified eClinical platform that brings clinical data collection, study management, and AI-powered study intelligence together in one environment. Designed for sponsors, CROs, and research institutions, TrialKit gives teams greater control over how studies are built, managed, and adapted throughout the clinical research lifecycle. The platform includes electronic data capture (EDC), ePRO/eCOA, eSource, eConsent, eTMF, randomization and trial supply management (RTSM), medical coding, adjudication, and more. Available through web and native mobile applications, TrialKit supports traditional, decentralized, and hybrid research with flexible options for collecting, managing, and analyzing clinical data. A core differentiator is Floyd, TrialKit's proprietary AI model, purpose-built to work directly within the platform. Floyd understands TrialKit's underlying data model, APIs, study architecture, and configuration, allowing it to support activities across the clinical study lifecycle. Its capabilities span protocol interpretation, study design and build, simulation, validation, and advanced analysis. From generating CRFs and study logic to testing configurations with synthetic participants and analyzing clinical data, Floyd helps teams evaluate study decisions, identify potential risks, and accelerate execution while maintaining human oversight. Beyond its technology, TrialKit offers a flexible commercial model through its Platform License Agreement (PLA), with predictable monthly pricing and no incremental change-order fees for routine study modifications. Combined with its unified architecture and self-service configuration capabilities, this approach gives organizations greater control over study operations, technology costs, and evolving research requirements. Built for studies of varying sizes and complexities, TrialKit brings together the tools, intelligence, and flexibility research teams need to manage clinical studies within a single platform.

Average Rating: 4.6/5.0

Total Reviews: 26

How Do G2 Users Rate TrialKit?

  • Data Centralization: 8.8/10 (Category avg: 8.7/10)
  • Quality of Support: 9.4/10 (Category avg: 8.6/10)
  • Documentation: 7.9/10 (Category avg: 8.4/10)
  • Site Management: 6.7/10 (Category avg: 8.6/10)

Who Is the Company Behind TrialKit?

Who Uses This Product?

  • Top Industries: Medical Devices
  • Company Size: 61% Small, 32% Medium

What Do G2 Reviewers Say About TrialKit?

AI-generated summary from verified user reviews

Pros
  • Users commend the excellent customer support from TrialKit, highlighting prompt and knowledgeable assistance from the team.
  • Users appreciate the ease of use of TrialKit, finding it straightforward for data entry and monitoring.
  • Users appreciate the robust features and support of TrialKit, effectively meeting their research study needs.
  • Users praise the excellent user interface of TrialKit, highlighting its ease of use and effective support resources.
  • Users love the access ease of TrialKit, allowing quick form adjustments without disrupting timelines.
Cons
  • Users find the documentation lacking, leading to confusion and difficulties in utilizing TrialKit's features effectively.
  • Users find the inadequate reporting in TrialKit cumbersome, impacting the ease of capturing key performance metrics.
  • Users find the sales and study development process unclear, leading to frustrations and delays in their experience.
  • Users find limited flexibility in TrialKit, wishing for easier customization options and improved dashboard functionality.
  • Users express frustration with the slow performance of TrialKit, citing delays and inefficiencies while handling large data sets.

What Are Recent G2 Reviews of TrialKit?

TrialHub

TrialHub is designed specifically for clinical research organizations, pharma, and biotech companies. More than just a feasibility platform, TrialHub simplifies trial design and strategic planning decisions by automating global Standard of Care (SoC) data and consolidating insights on epidemiology, diversity, patients’ unmet needs, trial performance, site availability, etc. into a single platform thanks to GenAI and validated data. 1. Standard of Care & patient insights: our automated database is used by the likes of Novartis, ICON, and Syneos to better understand the patient pathway and use this knowledge for protocol optimization and more precise country and site selection. Focused on all ex-US countries where claims data is not present and hard to obtain. 2. Country feasibility: our bespoke Feasibility Index helps experts select the best countries for their clinical trial based on specific recruitment goals. 3. Site selection: TrialHub helps strategists identify the best sites for their clinical trial so that patient recruitment can be completed on budget and on time. 4. AI powerhouse: TrialHub IQ is an advanced intelligent query tool that allows users to quickly analyze complex clinical data, offering precise answers and facilitating rapid, informed decision-making. Powered by AI and NLP technologies, it provides instant access to over 20 million PubMed articles and thousands of medical guidelines and global clinical registries.

Average Rating: 4.4/5.0

Total Reviews: 27

How Do G2 Users Rate TrialHub?

  • Data Centralization: 7.9/10 (Category avg: 8.7/10)
  • Quality of Support: 9.8/10 (Category avg: 8.6/10)
  • Documentation: 7.6/10 (Category avg: 8.4/10)
  • Site Management: 7.7/10 (Category avg: 8.6/10)

Who Is the Company Behind TrialHub?

Who Uses This Product?

  • Top Industries: Pharmaceuticals, Research
  • Company Size: 41% Medium, 33% Large

What Are Recent G2 Reviews of TrialHub?

Fusion eClinical Suite EDC

Axiom Fusion eClinical Suite is the most adaptable, Unified Platform that serves as the Connected Hub for all your Clinical Trial and operational data and reporting. Choose from 15+ unified modules on a single platform: EDC, DM, RTSM/IRT, CTMS, Inventory Management, ePRO, eConsent, Patient Portal, AE/SAE Tracking, Safety Database, Central/Local Lab, Imaging Management, eTMF, and 24/7 Project and Clinical Data Reporting. We are an embedded partner dedicated to the success of your study, offering managed services such as: Data Management, On-Demand Data Analytics, Biostatistics, Clinical Management, eTMF Management and Pharmacovigilance.

Average Rating: 3.4/5.0

Total Reviews: 56

How Do G2 Users Rate Fusion eClinical Suite EDC?

  • Data Centralization: 8.7/10 (Category avg: 8.7/10)
  • Quality of Support: 8.0/10 (Category avg: 8.6/10)
  • Documentation: 8.5/10 (Category avg: 8.4/10)
  • Site Management: 8.4/10 (Category avg: 8.6/10)

Who Is the Company Behind Fusion eClinical Suite EDC?

Who Uses This Product?

  • Top Industries: Research, Hospital & Health Care
  • Company Size: 65% Small, 19% Medium

What Are Recent G2 Reviews of Fusion eClinical Suite EDC?

What Are G2 Users Discussing About Fusion eClinical Suite EDC?

Clinical Conductor CTMS

Clinical Conductor CTMS is an industry-leading clinical trial management system (CTMS) trusted by health systems, hospitals, site networks, and dedicated research sites. It streamlines operational, financial, and regulatory workflows to improve efficiency and quality across the research lifecycle. Backed by Advarra's expert team with deep experience in research operations, Clinical Conductor offers true enterprise capabilities that enable organizations to scale—supporting growth, high study volumes, and multi-site management. The platform delivers comprehensive, end-to-end functionality, including strong financial management workflow management, protocol management, participant recruitment, visit tracking, scheduling, and financial reporting. Clinical Conductor also features exclusive, turnkey integrations with Advarra’s eReg and eSource systems, enhancing connectivity and driving greater efficiency across research workflows.

Average Rating: 4.1/5.0

Total Reviews: 8

How Do G2 Users Rate Clinical Conductor CTMS?

  • Data Centralization: 5.4/10 (Category avg: 8.7/10)
  • Quality of Support: 9.3/10 (Category avg: 8.6/10)
  • Documentation: 5.8/10 (Category avg: 8.4/10)
  • Site Management: 6.7/10 (Category avg: 8.6/10)

Who Is the Company Behind Clinical Conductor CTMS?

  • Seller: Advarra
  • Year Founded: 1983
  • HQ Location: Columbia, US
  • LinkedIn® Page: www.linkedin.com
    1,863 employees on LinkedIn®

Who Uses This Product?

  • Company Size: 88% Small, 13% Medium

What Are Recent G2 Reviews of Clinical Conductor CTMS?

Salesforce Life Sciences Cloud

Salesforce Life Sciences Cloud is an intelligent, AI-first end-to-end engagement platform that redefines how the clinical, medical, and commercial teams engage with patients, healthcare providers, clinical trial sites and care ecosystems to bring new therapies to market faster. Built on the deeply unified Platform, it enables pharma and medtech organizations to personalize customer interactions, streamline clinical operations, and improve patient outcomes with data, contextual insights, and trusted AI. Transform Clinical Trials - Automate personalized engagement, prescreening, and scheduling for efficient enrollment into clinical trials - Streamline clinical trial site and investigator selection with AI powered by comprehensive site performance data - Enable study teams and sites to manage and oversee clinical trials, ensuring timely and high quality clinical trials Reimagine HCP Engagement - Enable field teams with data-driven intelligence on a mobile-first application - Provide a hands-free experience to field teams with AI-powered audio briefings and voice based visit logging - Drive product adoption with 24x7 support for medical inquiries - Deliver impact during visits powered by pre-approved content - Manage schedules, samples, and signature captures with compliance built in the flow of work - Streamline order management including store checks and quoted orders, even offline Improve Patient Outcomes - Increase patient onboarding to latest therapies with seamless benefit (re)verification and financial assistance. - Take immediate actions based on AI-powered recommendations to boost patient adherence and prevent dropoffs Compliance at Every Step - Maximize efficiency with structured and unstructured data consolidated with zero-copy integration powered by Data 360 - Maintain adherence to global and regional regulations including HIPAA, GDPR, GxP, and FedRamp with Life Sciences Cloud - Set user-based permissions within your organization to control patient data visibility Open Ecosystem for Interoperability - Leverage AppExchange, AgentExchange, and the extensive network of partners across domains - Seamlessly integrate with Salesforce Customer 360 products like Slack, Marketing Cloud, Tableau, and Commerce Cloud - Bring rich industry data natively into the application via Data 360 from partners like H1, Viz.ai, and IQVIA to unlock precise insights and tailored recommendations

Average Rating: 4.1/5.0

Total Reviews: 38

Who Is the Company Behind Salesforce Life Sciences Cloud?

  • Seller: Salesforce
  • Company Website:
  • Year Founded: 1999
  • HQ Location: San Francisco, CA
  • LinkedIn® Page: www.linkedin.com
    89,711 employees on LinkedIn®
  • Ownership: NYSE:CRM

Who Uses This Product?

  • Top Industries: Hospital & Health Care
  • Company Size: 41% Large, 38% Medium

What Are Recent G2 Reviews of Salesforce Life Sciences Cloud?

Antidote

Antidote is a digital health company on a mission to accelerate the breakthroughs of new treatments by bridging the gap between medical research and the people who need it.

Average Rating: 4.7/5.0

Total Reviews: 5

How Do G2 Users Rate Antidote?

  • Quality of Support: 7.9/10 (Category avg: 8.6/10)

Who Is the Company Behind Antidote?

  • Seller: Antidote
  • Year Founded: 2006
  • HQ Location: London, GB
  • LinkedIn® Page: www.linkedin.com
    22 employees on LinkedIn®

Who Uses This Product?

  • Company Size: 60% Small, 40% Medium

What Are Recent G2 Reviews of Antidote?

What Are G2 Users Discussing About Antidote?

Datacapt

Join the New Clinical Trial Experience. Datacapt is a next-generation unified EDC platform designed for CROs, Sites, Sponsors and Participants in the Medical Device, Biotech and Pharmaceutical industry. Enjoy a modular, easy-to-use and powerful platform for your next on-site, hybrid or decentralized clinical trials. With a clean and intuitive interface, we provide enhanced accessibility, flexibility, and convenience empowering researchers to conduct clinical research efficiently and effectively!

Average Rating: 5.0/5.0

Total Reviews: 4

How Do G2 Users Rate Datacapt?

  • Data Centralization: 10.0/10 (Category avg: 8.7/10)
  • Quality of Support: 10.0/10 (Category avg: 8.6/10)

Who Is the Company Behind Datacapt?

  • Seller: Datacapt
  • Company Website:
  • Year Founded: 2019
  • HQ Location: Lyon, FR
  • LinkedIn® Page: www.linkedin.com
    19 employees on LinkedIn®

Who Uses This Product?

  • Company Size: 50% Small, 25% Large

What Are Recent G2 Reviews of Datacapt?

Clindex

A Clinical Data Management System (CDMS), Clinical Trial Management System (CTMS) and Electronic Data Capture System (EDC) all in one powerful, integrated solution.

Average Rating: 4.2/5.0

Total Reviews: 3

Who Is the Company Behind Clindex?

Who Uses This Product?

  • Company Size: 67% Medium, 33% Large

What Are Recent G2 Reviews of Clindex?

Emma Stein
ES
Researched and written by Emma Stein
Updated October 3, 2024