# Best Clinical Trial Management Systems - Page 2 *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 ## How Many Clinical Trial Management Systems Products Does G2 Track? **Total Products under this Category:** 98 ### 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 03, 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 - 98+ 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=2026-07-04T02%3A15%3A20Z&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=8b7f34633af790fe2cf2f018db7e027bfd72ccb30ba7ce3334af200f7bd539ea&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. [Loftware Cloud Clinical Trials](https://www.g2.com/products/loftware-cloud-clinical-trials/reviews) Loftware Cloud Clinical Trials (previously named Loftware Prisym 360) streamlines clinical supplies labeling – it’s built into our software’s DNA. Our solution simplifies complexities and shortens timelines to deliver GxP-compliant labeling with consistency, accuracy, and speed. **Average Rating:** 2.5/5.0 **Total Reviews:** 1 **How Do G2 Users Rate Loftware Cloud Clinical Trials?** - **Quality of Support:** 0.0/10 (Category avg: 8.5/10) - **Documentation:** 6.7/10 (Category avg: 8.4/10) **Who Is the Company Behind Loftware Cloud Clinical Trials?** - **Seller:** [Loftware](https://www.g2.com/sellers/loftware) - **Year Founded:** 1986 - **HQ Location:** Portsmouth, US - **Twitter:** @LoftwareInc (1,414 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/loftware (499 employees on LinkedIn®) **Who Uses This Product?** - **Company Size:** 100% Enterprise ### 2. [Octalsoft IWRS](https://www.g2.com/products/octalsoft-iwrs/reviews) Randomization and Trial Supply Management (RTSM) systems, often synonymous with Interactive Web Response System (IWRS), are critical for managing clinical trials efficiently. Octalsoft’s Next-Zen IWRS software is tailored to reflect the needs of modern clinical research while meeting the requirements of the stringent regulatory framework. Octalsoft IWRS reduces bias, ensures balanced treatment groups, and streamlines clinical supply tracking—delivering the right product to the right subject, on time. **Average Rating:** 4.5/5.0 **Total Reviews:** 1 **How Do G2 Users Rate Octalsoft IWRS?** - **Data Centralization:** 10.0/10 (Category avg: 8.6/10) - **Quality of Support:** 8.3/10 (Category avg: 8.5/10) **Who Is the Company Behind Octalsoft IWRS?** - **Seller:** [Octalsoft](https://www.g2.com/sellers/octalsoft) - **Year Founded:** 2007 - **HQ Location:** Herndon, US - **Twitter:** @Octalsoft_ (35 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/octalsoft?trk=fc_badge (68 employees on LinkedIn®) **Who Uses This Product?** - **Company Size:** 100% Small-Business #### What Are Recent G2 Reviews of Octalsoft IWRS? **"[Outstanding Team Support Makes All the Difference](https://www.g2.com/survey_responses/octalsoft-iwrs-review-12127044)"** **Rating:** 4.5/5.0 stars *— Vinayak D.* [Read full review](https://www.g2.com/survey_responses/octalsoft-iwrs-review-12127044) --- ### 3. [TrialMind](https://www.g2.com/products/trialmind/reviews) Overview: TrialMind by Keiji AI is an agentic AI platform purpose-built for clinical research. Unlike general-purpose AI tools, TrialMind is a domain-tuned foundation model specifically trained on biomedical and regulatory workflows — supporting every stage of the clinical trial lifecycle, from literature review and trial design through data analysis and regulatory reporting. Backed by 22+ peer-reviewed publications in Nature, NeurIPS, and JAMIA, and deployed in production at organizations like Guardant Health, Regeneron, and Mass General Brigham, TrialMind gives clinical researchers, biostatisticians, and HEOR teams the AI capabilities of a large team without adding headcount. Key Features: Systematic Literature Review (SLR) Agent PRISMA-compliant automation for literature search, screening, and evidence synthesis. Achieves 92–99% screening accuracy and reduces SLR timelines by 50–60% compared to manual methods. Data Science Assistant (DSA) A natural-language copilot for real-world data analytics. Generates SAS, R, and Python code — including SDTM/ADaM programming and TLF outputs — from plain-language prompts. No coding required. Trial Design & Optimization Agent Drafts and optimizes eligibility criteria using historical data from 400,000+ clinical trials. Powered by AutoTrial, Keiji AI's proprietary protocol design model. Digital Twin & Simulation Agent Generates synthetic patient data to simulate trial outcomes and test protocol modifications before execution — reducing costly amendments. Predictive Outcome Modeling (SPOT) Forecasts trial results and risk factors using sequential predictive modeling, helping teams make go/no-go decisions earlier and with greater confidence. Integrations: TrialMind connects securely to external data sources via the Model Context Protocol (MCP), including: PubMed & Embase ClinicalTrials.gov and 13 additional global registries Electronic Health Records (EHRs) Medidata Rave, Veeva Vault, and other EDC/CTMS systems via API Access is available through the Keiji AI platform or via the TrialMind API for embedding into existing workflows. Security & Compliance: SOC 2 Type II Certified ISO 27001 Certified HIPAA Compliant (BAAs in place) Secure-by-Design Architecture: The AI Control Plane operates exclusively on metadata — schemas and variable names. All sensitive clinical, genomic, and regulatory data remains within the customer's secure environment. Raw data never leaves your infrastructure. Full Audit Trail: Every interaction is logged with immutable records, supporting GxP regulatory inspections. ALCOA+ Principles: Attributable, Legible, Contemporaneous, Original, Accurate data integrity standards. Proven Results Oncology RWD feasibility for 20+ data scientists with turnaround times reduce from 6–8 weeks to 3–5 days (10x faster) Protocol authoring & RWD cohort extraction with protocol design time reduced from months to days Large patient dataset analysis Research previously infeasible — now possible Who Uses TrialMind? Heads of Biometrics & Biostatistics HEOR / Real-World Evidence (RWE) Teams Clinical Operations & Trial Design Leads Real-World Data (RWD) Vendors Mid-size and large Pharma/Biotech organizations (Phase 2/3+) Why TrialMind vs. Generic AI Domain-tuned model — Outperforms GPT-4, Claude, and Mistral on clinical trial benchmarks (published in NPJ Digital Medicine) 850K+ trial protocols indexed from 14 global registries; 1.3M+ clinical publications 22+ peer-reviewed publications — not marketing claims Production-proven at Guardant Health, Regeneron, MGB and other leading academic medical centers About Keiji AI Keiji AI was founded with a mission to accelerate clinical trials through AI. The company is led by Jimeng Sun, a professor with 500+ publications, and a team of clinical AI researchers with work published in Nature, Nature BME, Nature Communications, and top AI venues. Keiji AI is headquartered in the United States. **Average Rating:** 5.0/5.0 **Total Reviews:** 1 **How Do G2 Users Rate TrialMind?** - **Data Centralization:** 10.0/10 (Category avg: 8.6/10) - **Quality of Support:** 10.0/10 (Category avg: 8.5/10) **Who Is the Company Behind TrialMind?** - **Seller:** [Keiji AI](https://www.g2.com/sellers/keiji-ai) - **Year Founded:** 2023 - **HQ Location:** Seattle, US - **LinkedIn® Page:** https://www.linkedin.com/company/97415783/ (9 employees on LinkedIn®) **Who Uses This Product?** - **Company Size:** 100% Small-Business #### What Are Recent G2 Reviews of TrialMind? **"[Amazing Product Suite and a Truly Collaborative TrialMind Team](https://www.g2.com/survey_responses/trialmind-review-12550835)"** **Rating:** 5.0/5.0 stars *— Angela W.* [Read full review](https://www.g2.com/survey_responses/trialmind-review-12550835) --- ### 4. [Agentforce Life Sciences (formerly Salesforce Life Sciences Cloud)](https://www.g2.com/products/agentforce-life-sciences-formerly-salesforce-life-sciences-cloud/reviews) Agentforce Life Sciences (formerly 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 Agentforce 360 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 - 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 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:** 5.0/5.0 **Total Reviews:** 1 **Who Is the Company Behind Agentforce Life Sciences (formerly Salesforce Life Sciences Cloud)?** - **Seller:** [Salesforce](https://www.g2.com/sellers/salesforce) - **Company Website:** https://www.salesforce.com/ - **Year Founded:** 1999 - **HQ Location:** San Francisco, CA - **Twitter:** @salesforce (579,511 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/3185/ (83,223 employees on LinkedIn®) **Who Uses This Product?** - **Company Size:** 100% Enterprise #### What Are Recent G2 Reviews of Agentforce Life Sciences (formerly Salesforce Life Sciences Cloud)? **"[Powerful, Simple, and Highly Recommended](https://www.g2.com/survey_responses/agentforce-life-sciences-formerly-salesforce-life-sciences-cloud-review-12790133)"** **Rating:** 5.0/5.0 stars *— Andriu U.* [Read full review](https://www.g2.com/survey_responses/agentforce-life-sciences-formerly-salesforce-life-sciences-cloud-review-12790133) --- ### 5. [Agentic AI Assistant](https://www.g2.com/products/agentic-ai-assistant/reviews) Clinion’s Agentic AI Assistant changes how teams interact with clinical trial data. Users can simply ask questions and get instant answers drawn directly from study data, protocol context, and operational workflows, instead of navigating through complex datasets. Powered by a system of specialized agents, it interprets intent, connects it to the right data source, and delivers responses that are grounded, traceable, and ready to use. What can you expect? ● Ask questions, get direct answers Interact with study data, protocol details, and operational metrics using natural language. ● Understands study context Maps questions to protocol structure, CRFs, and metadata to return relevant outputs. ● Specialized agents working in the background Different agents handle protocol logic, clinical data, and operations to ensure accuracy. ● Responses you can trust Every answer is grounded in study data with clear traceability and no cross-study overlap. ● Works inside your EDC Access insights in real time without switching tools or waiting on data teams. ● Ready from day one Automatically builds a study-specific knowledge base as soon as the study is set up. Impact Faster access to answers across teams Reduced reliance on manual data pulls More confident decisions with traceable outputs **Who Is the Company Behind Agentic AI Assistant?** - **Seller:** [Clinion](https://www.g2.com/sellers/clinion-e18ccd88-cb44-4bcb-a5cf-8a814664dc7a) - **Year Founded:** 2010 - **HQ Location:** Austin, US - **Twitter:** @clinion (54 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/clinion-eclinical-platform/?viewAsMember=true (64 employees on LinkedIn®) ### 6. [BizNET](https://www.g2.com/products/sarjen-system-biznet/reviews) Sarjen provides a suite of GxP-compliant software to streamline drug development. This includes automated CTMS for the efficient management of both early-phase and late-phase clinical trials, alongside a specialized Bioanalytical LIMS. These integrated solutions ensure end-to-end data integrity, accelerate workflows, and maintain audit-readiness across the entire research lifecycle. **Who Is the Company Behind BizNET?** - **Seller:** [Sarjen System](https://www.g2.com/sellers/sarjen-system) - **Year Founded:** 1998 - **HQ Location:** N/A - **LinkedIn® Page:** https://www.linkedin.com/company/1007381 (364 employees on LinkedIn®) ### 7. [Catchtrial eConsent](https://www.g2.com/products/catchtrial-econsent/reviews) Catchtrial® eConsent by Medigen Suite is an electronic informed consent platform that lets participants review and sign consent from anywhere using telemedicine-inspired technology. Compatible with Android and iOS, it removes the need for on-site visits and delivers a mobile-first experience for patients. Sponsors, CROs, biotech, pharmaceutical, and medical device organizations use Catchtrial® eConsent to streamline enrollment, reduce paper-based processes, and improve protocol adherence across decentralized, hybrid, and site-based studies. The platform maintains FDA 21 CFR Part 11, GDPR, HIPAA, and ICH-GCP compliance for global clinical research. **Who Is the Company Behind Catchtrial eConsent?** - **Seller:** [Meditrial Europe](https://www.g2.com/sellers/meditrial-europe-7178e686-2b50-4d24-8b4a-5d38db167103) - **Year Founded:** 2008 - **HQ Location:** Zug, Switzerland - **LinkedIn® Page:** https://www.linkedin.com/company/meditrial-today/ (90 employees on LinkedIn®) ### 8. [Catchtrial EDC+](https://www.g2.com/products/catchtrial-edc/reviews) Catchtrial EDC+ by Medigen Suite is a next-generation EDC software platform designed for modern clinical trials. It unifies electronic data capture, eCRF design, medical imaging (DICOM), risk-based monitoring, safety adjudication, analytics, and AI-driven insights into one secure, compliant environment. Built for sponsors, CROs, and research organizations, Catchtrial helps teams accelerate study execution, improve data quality, ensure regulatory compliance, and deliver approval-ready clinical evidence. The platform also supports ePRO, eCOA, eConsent, and decentralized trial capabilities for seamless clinical data capture across all study phases. **Who Is the Company Behind Catchtrial EDC+?** - **Seller:** [Meditrial Europe](https://www.g2.com/sellers/meditrial-europe-7178e686-2b50-4d24-8b4a-5d38db167103) - **Year Founded:** 2008 - **HQ Location:** Zug, Switzerland - **LinkedIn® Page:** https://www.linkedin.com/company/meditrial-today/ (90 employees on LinkedIn®) ### 9. [Chronicles Central Review Share](https://www.g2.com/products/chronicles-central-review-share/reviews) Secure portal for central readers, KOLs, and investigators to review and share data and documents. • Built-in DICOM anonymization, centralized imaging assessment (MRI/CT), and remote monitoring. • Controlled reviewer access. • eCRF-like report forms. • Collaboration tools to support central review processes. **Who Is the Company Behind Chronicles Central Review Share?** - **Seller:** [Chronicles Research Team](https://www.g2.com/sellers/chronicles-research-team) - **Year Founded:** 2021 - **HQ Location:** N/A - **LinkedIn® Page:** https://www.linkedin.com/company/chronicles-research-team/ (3 employees on LinkedIn®) ### 10. [Chronicles Clinical Trial Management System CTMS](https://www.g2.com/products/chronicles-clinical-trial-management-system-ctms/reviews) Clinical Trial Management System is a complex platform to plan, track, and control R&D activities across trials, sites, and vendors. • Project planning, milestones, Gantt-style charts, risk and issue tracking. • Sites, investigators, and vendors management. • Training management. • Electronic documents workflows. • Dashboards and electronic reports for operational oversight and inspection readiness. **Who Is the Company Behind Chronicles Clinical Trial Management System CTMS?** - **Seller:** [Chronicles Research Team](https://www.g2.com/sellers/chronicles-research-team) - **Year Founded:** 2021 - **HQ Location:** N/A - **LinkedIn® Page:** https://www.linkedin.com/company/chronicles-research-team/ (3 employees on LinkedIn®) ### 11. [Chronicles EDC / eCRF with RTSM](https://www.g2.com/products/chronicles-edc-ecrf-with-rtsm/reviews) Chronicles eCRF is a configurable SaaS solution which may be set up by clients in strict compliance with the protocol in both interventional (Phase I-IV and BE/BA) studies and non-interventional programs. • Integrated randomization, stratification and blinding. • Built-in trial supply management tools. • Study-specific form builder with edit checks, lab ranges, and multi-language support. • MedDRA and ATC coding, CDISC/CDASH-ready datasets. • Compatibility with modern statistical software such as SAS, R, SPSS, Excel, etc. **Who Is the Company Behind Chronicles EDC / eCRF with RTSM?** - **Seller:** [Chronicles Research Team](https://www.g2.com/sellers/chronicles-research-team) - **Year Founded:** 2021 - **HQ Location:** N/A - **LinkedIn® Page:** https://www.linkedin.com/company/chronicles-research-team/ (3 employees on LinkedIn®) ### 12. [CleanWEB](https://www.g2.com/products/cleanweb/reviews) A global solution for the electronic management of clinical trials EDC – IWRS – CTMS – CDMS – ePRO – IoTs – eTMF … CleanWEB is a secure Internet platform dedicated to managing national or international clinical electronic studies, registries and cohorts, mono or multi-centric. It is especially made for projects of all kinds: clinical trial from phase I to IV, real-life based studies, veterinary studies, epidemiological studies. Certifications : CDISC ODM – ISO 9001:2008 – 21 CFR Part 11 Compliance **Who Is the Company Behind CleanWEB?** - **Seller:** [Telemedicine Technologies](https://www.g2.com/sellers/telemedicine-technologies) - **Year Founded:** 2000 - **HQ Location:** Boulogne Billancourt, FR - **LinkedIn® Page:** https://www.linkedin.com/company/telemedicine-technologies (39 employees on LinkedIn®) ### 13. [Clinical Trials for HubSpot & Salesforce](https://www.g2.com/products/clinical-trials-for-hubspot-salesforce/reviews) Clinical Trials for HubSpot and Salesforce integrates public clinical trial data into your CRM, adding unique search functions, reporting capabilities, and automation. No separate software, no downtime for a learning curve – just clean data that drives business. **Who Is the Company Behind Clinical Trials for HubSpot & Salesforce?** - **Seller:** [The Bracken Group](https://www.g2.com/sellers/the-bracken-group) - **HQ Location:** Newtown, US - **LinkedIn® Page:** https://www.linkedin.com/company/thebrackengroup (61 employees on LinkedIn®) ### 14. [Clinicubes CTMS](https://www.g2.com/products/clinicubes-ctms/reviews) Centralized software which provides ways to manage, track, and document throughout the clinical trials process. **Who Is the Company Behind Clinicubes CTMS?** - **Seller:** [BGO Software](https://www.g2.com/sellers/bgo-software) - **Year Founded:** 2008 - **HQ Location:** London, GB - **Twitter:** @BGOSoftware (171 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/bgo-software (78 employees on LinkedIn®) ### 15. [Clinion CTMS](https://www.g2.com/products/clinion-ctms/reviews) Clinion CTMS An intuitive, integrated clinical trial management system for sponsors and CROs. Clinion CTMS provides centralized visibility and control over clinical trial operations. Built as part of a unified platform, it integrates natively with Clinion EDC, RTSM, and eTMF, enabling real-time access to clinical, operational, and financial data across the study lifecycle. What can you expect? ● Centralized Trial Oversight Manage sites, enrollment, milestones, deviations, and study progress from a single system. ● Deep Integration Across the Platform Connect seamlessly with EDC and RTSM to ensure consistent data and reduce manual reconciliation. ● Real-Time Tracking and Alerts Monitor study milestones and activities with dashboards and notifications to stay on schedule. ● Financial and Operational Control Track budgets, invoices, and payments with full visibility into trial finances. ● Configurable Workflows Adapt the system to your processes with flexible configurations, approval flows, and notifications. ● Easy to Use and Quick to Deploy Intuitive interface designed to reduce training time and accelerate adoption. Quick facts Central hub for clinical, operational, and financial data Supports Phase I to Phase IV trials 100% web-based and securely hosted Compliant with 21 CFR Part 11 and GDPR **Who Is the Company Behind Clinion CTMS?** - **Seller:** [Clinion](https://www.g2.com/sellers/clinion-e18ccd88-cb44-4bcb-a5cf-8a814664dc7a) - **Year Founded:** 2010 - **HQ Location:** Austin, US - **Twitter:** @clinion (54 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/clinion-eclinical-platform/?viewAsMember=true (64 employees on LinkedIn®) ### 16. [Clinion eConsent](https://www.g2.com/products/clinion-econsent/reviews) Clinion eConsent replaces manual consent processes with a digital system designed to improve patient onboarding and ensure compliance. Built within a unified platform, it enables real-time tracking, secure documentation, and seamless integration with Clinion EDC. What can you expect? ● Flexible Consent Models Support site-based, remote, and ePRO-linked consent workflows based on study needs. ● Faster Patient Enrollment Reduce onboarding timelines with digital consent and automated re-consenting for protocol updates. ● Real-Time Tracking and Oversight Monitor consent status and patient progress with complete visibility. ● ICF Version Control and Audit Trail Track consent versions with time-stamped signatures and maintain compliance-ready records. ● Improved Patient Experience Use multimedia-enabled consent forms to support better understanding and engagement. ● Seamless EDC Integration Automatically enroll subjects and sync consent data directly with Clinion EDC. Impact Faster patient enrollment timelines Reduced paperwork and manual tracking Improved compliance with audit-ready documentation **Who Is the Company Behind Clinion eConsent?** - **Seller:** [Clinion](https://www.g2.com/sellers/clinion-e18ccd88-cb44-4bcb-a5cf-8a814664dc7a) - **Year Founded:** 2010 - **HQ Location:** Austin, US - **Twitter:** @clinion (54 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/clinion-eclinical-platform/?viewAsMember=true (64 employees on LinkedIn®) ### 17. [Clinpal](https://www.g2.com/products/clinpal/reviews) A new breed of cloud-based, patient-centric data capture solutions designed to handle both ePRO and EDC on BYOD. **Who Is the Company Behind Clinpal?** - **Seller:** [eClinicalHealth](https://www.g2.com/sellers/eclinicalhealth) - **Year Founded:** 2002 - **HQ Location:** Bottisham, GB - **LinkedIn® Page:** https://www.linkedin.com/company/cambridge-cognition/ (69 employees on LinkedIn®) ### 18. [Clinsoft](https://www.g2.com/products/clinsoft/reviews) 21 CFR Part 11 Compliant, Web-Enabled eClinical Suite with integrated Clinical Trial Management. **Who Is the Company Behind Clinsoft?** - **Seller:** [Innovate Research](https://www.g2.com/sellers/innovate-research) - **Year Founded:** 2014 - **HQ Location:** Noida, IN - **LinkedIn® Page:** https://www.linkedin.com/company/3600305/ (42 employees on LinkedIn®) ### 19. [ClinVigilant eClinical](https://www.g2.com/products/clinvigilant-eclinical/reviews) Streamline your clinical studies with ClinVigilant, your global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us thanks to our: ♦ Fast EDC set-up (less than 4 weeks). ♦ Cost-effectiveness. ♦ 3rd party integrations (including legacy systems). Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA. The ClinVigilant® eClinical suite includes: EDC, eCRF, CTMS, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem. How simple and user-friendly is it? Ask for a demo to find out! Clinvigilant💊, your one-stop 🌐solutions provider for ☁️clinical trials . Enquiries \> bd@clinvigilant.com **Who Is the Company Behind ClinVigilant eClinical?** - **Seller:** [ClinVigilant](https://www.g2.com/sellers/clinvigilant) - **Year Founded:** 2017 - **HQ Location:** Dartford, GB - **LinkedIn® Page:** https://www.linkedin.com/company/clinvigilantresearch (19 employees on LinkedIn®) ### 20. [Cloudbyz CTMS](https://www.g2.com/products/cloudbyz-ctms/reviews) Cloudbyz's Clinical Trial Management System (CTMS) is a cloud-based clinical trial operations management solution natively built on Salesforce's platform. It enables end-to-end management across all phases of the clinical study with real-time visibility and analytics across study planning, start up, study management, and close out. **Who Is the Company Behind Cloudbyz CTMS?** - **Seller:** [Cloudbyz](https://www.g2.com/sellers/cloudbyz) - **Year Founded:** 2014 - **HQ Location:** Naperville, US - **Twitter:** @cloudbyz (399 Twitter followers) - **LinkedIn® Page:** https://www.linkedin.com/company/cloudbyz (100 employees on LinkedIn®) ### 21. [CTMS](https://www.g2.com/products/clinevo-technologies-ctms/reviews) Clinevo Clinical Trial Management System (CTMS) is a cloud based, highly configurable, "end-to-end platform which" helps manage all aspects of clinical trials including : Site Monitoring Visits Milestones - Planning and Tracking Activities - Tasks & Deviations Payments - Site & Investigator Investigational Product (IP) Tracking & Inventory (IWRS) Patient Recruitment & Randomization (IWRS) Patient Visits - Scheduling and Tracking Site Selection, Site Initiation, Investigator Selection Master Data Management (Sites, Investigators) Regulatory documents & Compliance Tracking Study Budgets & Training Management Adverse Event Tracking and many more. Clinevo Clinical Trial Management System (CTMS) meets the regulatory guidelines including security, access control, change controls, audit trails, and the best system validation. **Who Is the Company Behind CTMS?** - **Seller:** [Clinevo Technologies](https://www.g2.com/sellers/clinevo-technologies) - **Year Founded:** 2016 - **HQ Location:** Bangalore, IN - **LinkedIn® Page:** https://www.linkedin.com/company/13426084 (98 employees on LinkedIn®) ### 22. [Curebase](https://www.g2.com/products/curebase/reviews) Curebase is the modern eClinical platform built for flexibility, usability, and full-study oversight, empowering sponsors, CROs, and sites to launch faster, adapt confidently, and deliver better participant experiences with next-gen ePRO, eConsent, engagement tools, and integrated EDC. **Who Is the Company Behind Curebase?** - **Seller:** [Curebase](https://www.g2.com/sellers/curebase) - **Year Founded:** 2017 - **HQ Location:** San Francisco, US - **LinkedIn® Page:** https://www.linkedin.com/company/curebase/ (41 employees on LinkedIn®) ### 23. [Datacapt](https://www.g2.com/products/datacapt/reviews) 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! **Who Is the Company Behind Datacapt?** - **Seller:** [Datacapt](https://www.g2.com/sellers/datacapt) - **Year Founded:** 2019 - **HQ Location:** Lyon, FR - **LinkedIn® Page:** https://www.linkedin.com/company/datacapt (19 employees on LinkedIn®) ### 24. [Ddots CREDIT](https://www.g2.com/products/ddots-credit/reviews) Ddots allows users to track adherence to protocol requirements each and every step of the way from patient treatment plans to required regulatory notifications. **Who Is the Company Behind Ddots CREDIT?** - **Seller:** [Ddots](https://www.g2.com/sellers/ddots) - **Year Founded:** 1995 - **HQ Location:** Ypsilanti, US - **LinkedIn® Page:** https://www.linkedin.com/company/ddots/ (30 employees on LinkedIn®) ### 25. [Delve Health](https://www.g2.com/products/delve-health/reviews) Delve Health is a clinical trial compliance and patient engagement company. We combine eCOA/ePRO, wearable device integration, real-time analytics, and Concierge-as-a-Service™ to help sponsors, CROs, and research sites run studies with higher completion rates, stronger retention, and cleaner data. Based in Minneapolis, serving programs across North America, Europe, Asia, and MENA. **Who Is the Company Behind Delve Health?** - **Seller:** [Delve Health](https://www.g2.com/sellers/delve-health) - **HQ Location:** Plymouth, MN - **Twitter:** @DelveHealth (544 Twitter followers) ## 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)