# Best Clinical Trial Management Systems - Page 6

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

**Total Products under this Category:** 102

### Category Stats (Aug 2026)

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

_Last updated: August 01, 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)

**Sponsored**

### SimplyMerit

SimplyMerit® is a compensation management software solution that enables HR teams, executives, and managers to plan and administer compensation programs with greater accuracy, efficiency, and security. It replaces manual spreadsheets with a centralized application designed to support merit budgets, annual bonus pools, and equity grants across global organizations. With SimplyMerit, organizations gain transparency into compensation decisions while reducing errors and administrative burden. HR leaders configure rules that match their business needs, managers make data-driven pay decisions, and employees see the full value of their pay through personalized Total Rewards Statements and a dedicated employee portal. SimplyMerit is particularly valuable for organizations managing multi-currency workforces, running complex approval workflows, or seeking to eliminate the risks of spreadsheet-based compensation cycles. Enterprise teams choose SimplyMerit for depth rather than breadth. HCM suites are broad by design and comparatively shallow in merit, bonus, and equity planning. SimplyMerit supplies that depth alongside the systems already in place, with no core HR replacement project: layered approval hierarchies backed by a full audit trail, consolidated multi-currency budgets across entities and regions, granular role-based permissions, and configuration that adapts as compensation strategy changes. Large employers run SimplyMerit as a dedicated planning layer while their HCM remains the system of record. Implementation does not depend on integration readiness. Clients who arrive with nothing more than a messy spreadsheet have gone live in under five days, because SimplyMerit maps and transforms the data it receives rather than asking clients to reformat it first. API connectors are added where systems expose access, and they can follow go-live instead of gating it. KEY FEATURES AND CAPABILITIES Compensation planning: manage merit increases, bonuses, and equity grants in one application. Dynamic field mapping: send an export from any system and SimplyMerit maps and transforms the fields, with no HRIS change and no reformatting required. API connectors: direct connections where HRIS and payroll systems expose API access, with your team mapping fields once. New connectors are built as clients bring their systems. Global budget consolidation: automatic currency conversion and prorations from configurable business rules, with a single consolidated view across entities and regions. Approval hierarchies: route pay decisions through custom approval paths, with executive approvals recorded as a system of record for auditability. Live budget tracking: managers see allocations against spend as they enter recommendations. Configuration support: adjust rules, guidelines, and workflows as compensation strategy changes, working with compensation professionals rather than a ticket queue. Total Rewards Statements: generate and securely distribute personalized summaries of total compensation. Employee portal: a fully customizable portal where employees view compensation details, Total Rewards Statements, and compensation statements, including personalized total rewards dashboards. Retained award history: prior awards and statements stay available to employees, with clients deciding how much history to load and retain. Year-round employee access: extend the portal beyond the annual cycle as a configurable setting, so employees can revisit their total rewards and history between planning cycles. Mobile-ready application: support managers wherever they work with a responsive interface. Data security: enterprise-grade security, granular role-based access, and GDPR compliance. USE CASES HR and compensation teams running annual or mid-year compensation cycles. Enterprises needing compensation depth alongside an existing HCM without replacing core HR. Organizations managing multi-currency workforces across multiple entities and geographies. Companies with multi-level approval hierarchies and audit requirements. Organizations looking to reduce risk and eliminate spreadsheet-driven processes. Teams that need to launch quickly without waiting on an integration project. Employers strengthening year-round pay communication as transparency expectations rise. Businesses seeking better visibility and governance over compensation decisions. By streamlining compensation planning, SimplyMerit helps organizations improve accuracy, reduce risk, and deliver a better employee experience. Leaders gain confidence in budget management, managers make fairer pay decisions with real-time visibility, and employees understand the full value of their rewards.

[Visit website](https://www.g2.com/external_clickthroughs/record?secure%5Bad_program%5D=ppc&secure%5Bad_slot%5D=category_product_list_llm&secure%5Bcategory_id%5D=446&secure%5Bchosen_at%5D=2026-08-02T17%3A01%3A53Z&secure%5Bdisplayable_resource_id%5D=1008699&secure%5Bdisplayable_resource_type%5D=Category&secure%5Bmedium%5D=sponsored&secure%5Bplacement_reason%5D=retargeted_product&secure%5Bplacement_resource_ids%5D%5B%5D=69694&secure%5Bprioritized%5D=false&secure%5Bproduct_id%5D=69694&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%3Fpage%3D6&secure%5Btoken%5D=6ac1ffd46de1e2e225238f97a1277453d7d3213f5a2ac91516898f4b1d401ca7&secure%5Burl%5D=https%3A%2F%2Fmorganhr.com%2Fschedule-a-demo&secure%5Burl_type%5D=book_demo)

### [Medable](https://www.g2.com/products/medable/reviews)

At Medable, we believe health and access to clinical trials is a human right, and participation should be easy. We understand that inclusive medicine removes barriers to clinical trials creating new trial efficiencies that amplify science, enabling you to bring treatments to market faster than ever before. Amplify science with the No. 1 rated leader in DCT Rated #1 DCT Provider by Everest’s PEAK Matrix® Assessment 2021 Extensible Platform Built to securely scale your studies today or in the future with a unified modern cloud infrastructure and flexible modular apps. Patient-Centric Services Put the patient at the center of care. With a range of DtP services including home health nursing, Connected Devices and Remote Sites, make participating in a trial as convenient as possible. Smart Data for Better Decisions Seamlessly integrates with hundreds of external data sources across: IRT, EDC, CTMS, EMR, Labs, Sensors, Wearables, Custom Systems, etc. Trusted DCT Ecosystem The largest and most trusted ecosystem of DCT partners including: CROs, System Integrators, Data & Tech, Devices - provide access to the smartest path forward for your organization and studies as they scale. DCT Training & Expertise The easiest way to increase your organization’s DCT expertise and start-up your studies efficiently. The Medable Platform Ecosystem Simplify the trial experience with a platform purpose built by clinicians, patient advocates, and technology experts. Because our platform is built from the ground up, not stitched together, we’re able to offer an intuitive experience for all stakeholders that integrates with any eClinical system and delivers real-time data insights for monitoring, safety, and efficacy.

#### Who Is the Company Behind Medable?

- **Seller:** [Medable](https://www.g2.com/sellers/medable)
- **Year Founded:** 2016
- **HQ Location:** Palo Alto, California, United States
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=f706398d468b84e461a843935481116cffc2bea386027c29979a2dbcc5aaba0f&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fmedable-inc-&secure%5Burl_type%5D=linkedin_company_website)  
327 employees on LinkedIn®

### [Medigen Suite](https://www.g2.com/products/medigen-suite/reviews)

Medigen Suite is Meditrial's eClinical platform for streamlined global clinical operations. Designed as a modular clinical trial software, it supports medical device companies, biotechnology firms, pharmaceutical sponsors, CROs, and academic research institutions across all study phases. - Catchtrial EDC delivers comprehensive electronic data capture with ePRO, eDiary, eConsent, and decentralized trial (DCT) capabilities for seamless patient engagement and remote data collection. - Maptrial CTMS provides full clinical trial management, including site monitoring, study tracking, and operational oversight for efficient trial execution. - Mastertrial LMS+ delivers scalable digital training for investigators and research teams to accelerate site activation and ensure regulatory compliance. Medigen Suite also offers a lightweight, cost-effective configuration for rapid study startup and feasibility assessments, making it accessible for organizations of any size.

#### Who Is the Company Behind Medigen Suite?

- **Seller:** [Meditrial Europe](https://www.g2.com/sellers/meditrial-europe-7178e686-2b50-4d24-8b4a-5d38db167103)
- **Year Founded:** 2008
- **HQ Location:** Zug, Switzerland
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=621a0ba793b3f97bc137247edee67f076715cb7e6df33e6c73cd8590c4193685&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fmeditrial-today%2F&secure%5Burl_type%5D=linkedin_company_website)  
90 employees on LinkedIn®

### [MediLake](https://www.g2.com/products/medilake/reviews)

CDISC-based fast eCRF production with AI technology. Provides customized EDCs. GAMP5 certification as an integrated platform for clinical trial data management. 21 CFR Part 11, Annex 11 Certification ISO900:2015 Certification 24/7 Global Service Support Team Quick trial start and affordability compared to other systems

#### Who Is the Company Behind MediLake?

- **Seller:** [Clupea](https://www.g2.com/sellers/clupea)
- **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=7886df2ed926834e5eb248c77dcfa8e5c815d3ab1f0fe3132ced0dba45868834&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2FNo-Linkedin-Presence-Added-Intentionally-By-DataOps&secure%5Burl_type%5D=linkedin_company_website)  
1 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=b96f303eeb04c30b73c016b6a4bf92685efb2262e62b6bff01f769fe4dd37db9&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fmonsana-ai%2F&secure%5Burl_type%5D=linkedin_company_website)  
3 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=381113aa455ffabffb94c3c250a5dc2f4c8d62f142dcff191be52cf75d9560ec&secure%5Burl%5D=http%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fcareevolution-inc&secure%5Burl_type%5D=linkedin_company_website)  
80 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=e1646a603961c3954379fbbd8a9d08ec768bea02110c8a8d783e8301cb63fd0b&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fwemedoo%2F&secure%5Burl_type%5D=linkedin_company_website)  
37 employees on LinkedIn®
- **Phone:** +41 41 740 0124

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=927ba00c528f609145554c5ab263424650a2d65f734b195c9769d66a15e169b2&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Ftri-the-rbqm-experts&secure%5Burl_type%5D=linkedin_company_website)  
98 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=35c6b7f4658bad6efb0cf8e7e29037172068fb982b7248549e8ddd0151da5b76&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fllc-atlant-systems%2F&secure%5Burl_type%5D=linkedin_company_website)  
2 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=2a827410e1edc1863bd5ebdf496276a79517c628d2e2f646de57473b02d8694b&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Frealtime-ctms-software-solutions&secure%5Burl_type%5D=linkedin_company_website)  
96 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=8742163cddf17ef9785dce00a6a578b962c4012e164edbf7d67755292e385e2d&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fscienta-lab%2F&secure%5Burl_type%5D=linkedin_company_website)  
19 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=7886df2ed926834e5eb248c77dcfa8e5c815d3ab1f0fe3132ced0dba45868834&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2FNo-Linkedin-Presence-Added-Intentionally-By-DataOps&secure%5Burl_type%5D=linkedin_company_website)  
1 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=07227a1778320d581a933faede2fe2a27240a204d775a3c442921ab02225373b&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Ftrialstat%2F&secure%5Burl_type%5D=linkedin_company_website)  
12 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=05b0c9c86634940102147facb3f3ee40c8efe02300dba703bc1e959544fb8e8d&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fsharecare-inc&secure%5Burl_type%5D=linkedin_company_website)  
3,821 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=bde7fa431decca2e380ff9611be18c0a82bbfff0cbfddb84e6176169b1cccd57&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fstudypages-platform%2F&secure%5Burl_type%5D=linkedin_company_website)  
11 employees on LinkedIn®

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=47d963310f762b66335f3aff82451161c65f020acad4935f446b54a037550a22&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fprecision-digital-health-inc&secure%5Burl_type%5D=linkedin_company_website)  
24 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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