# Best Electronic Trial Master File (eTMF) Software - Page 2

## How Many Electronic Trial Master File (eTMF) Software Products Does G2 Track?

**Total Products under this Category:** 39

### Category Stats (Jul 2026)

- **Average Rating:** 4.4/5 The average rating of products in this category, based on all submitted ratings

_Last updated: July 14, 2026_

## How Does G2 Rank Electronic Trial Master File (eTMF) Software Products?

**Why You Can Trust G2's Software Rankings:**

- 30 Analysts and Data Experts
- 2,300+ Authentic Reviews
- 39+ 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 Electronic Trial Master File (eTMF) Software
 ![G2 Grid® for Electronic Trial Master File (eTMF) Software plotting products by satisfaction and market presence](https://www.g2.com/categories/electronic-trial-master-file-etmf/grids.png?focus%5B%5D=18510&focus%5B%5D=2083&focus%5B%5D=2511&focus%5B%5D=94249&focus%5B%5D=1315744&focus%5B%5D=134478&focus%5B%5D=122044)

Highlighted products: MasterControl Quality Management System, Egnyte, Veeva Vault, Viedoc, Kivo, Clinical Research Suite, and ACE.

Underlying data: [Grid® JSON](https://www.g2.com/categories/electronic-trial-master-file-etmf/grids.json?focus%5B%5D=mastercontrol-quality-management-system&focus%5B%5D=egnyte&focus%5B%5D=veeva-vault&focus%5B%5D=viedoc&focus%5B%5D=kivo&focus%5B%5D=clinical-research-suite&focus%5B%5D=psc-software-ace)

[
Chronicles Clinical Trial...
](https://www.g2.com/products/chronicles-clinical-trial-management-system-ctms/reviews)

By [Chronicles Research Team](https://www.g2.com/sellers/chronicles-research-team)

[

0/5(0)

](https://www.g2.com/products/chronicles-clinical-trial-management-system-ctms/reviews)

Product Description

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 i

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=a5e8dfe22e557369bd7911d85f9f064dea44b989b80ce9bd4ef3e2306ce2c530&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fchronicles-research-team%2F&secure%5Burl_type%5D=linkedin_company_website)  
3 employees on LinkedIn®

[
Chronicles Electronic Trial...
](https://www.g2.com/products/chronicles-electronic-trial-master-file-etmf/reviews)

By [Chronicles Research Team](https://www.g2.com/sellers/chronicles-research-team)

[

0/5(0)

](https://www.g2.com/products/chronicles-electronic-trial-master-file-etmf/reviews)

Product Description

Electronic Trial Master File for compliant document storage, workflows, and inspection readiness. • Templates, versioning, electronic signatures, and role-based access. • QC workflows and audit tr

### [Chronicles Electronic Trial Master File eTMF](https://www.g2.com/products/chronicles-electronic-trial-master-file-etmf/reviews)

Electronic Trial Master File for compliant document storage, workflows, and inspection readiness. • Templates, versioning, electronic signatures, and role-based access. • QC workflows and audit trails aligned with GxP and 21 CFR Part 11 requirements.

#### Who Is the Company Behind Chronicles Electronic Trial Master File eTMF?

- **Seller:** [Chronicles Research Team](https://www.g2.com/sellers/chronicles-research-team)
- **Year Founded:** 2021
- **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=a5e8dfe22e557369bd7911d85f9f064dea44b989b80ce9bd4ef3e2306ce2c530&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fchronicles-research-team%2F&secure%5Burl_type%5D=linkedin_company_website)  
3 employees on LinkedIn®

[
CleanWEB
](https://www.g2.com/products/cleanweb/reviews)

By [Telemedicine Technologies](https://www.g2.com/sellers/telemedicine-technologies)

[

0/5(0)

](https://www.g2.com/products/cleanweb/reviews)

Product Description

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 internation

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=d6dc08dc2eba2884f9f992af38955bd8228e1e57d715af006f3ebde75d8284b3&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Ftelemedicine-technologies&secure%5Burl_type%5D=linkedin_company_website)  
39 employees on LinkedIn®

[
Clindex
](https://www.g2.com/products/clindex/reviews)

By [Fortress Medical Systems](https://www.g2.com/sellers/fortress-medical-systems)

[

4.2/5(3)

](https://www.g2.com/products/clindex/reviews)

Product Description

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

### [Clindex](https://www.g2.com/products/clindex/reviews)

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

#### How Do G2 Users Rate Clindex?

- **Ease of Use:** 8.3/10 (Category avg: 8.9/10)

#### Who Is the Company Behind Clindex?

- **Seller:** [Fortress Medical Systems](https://www.g2.com/sellers/fortress-medical-systems)
- **Year Founded:** 1997
- **HQ Location:** Hopkins, US
- **Twitter:** @plista  
1,389 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=fb8cba0bd4d1402ea2fe98aee7926a4d7572a4e66031cd6a699b076cb4a652e7&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F3134457%3Ftrk%3Dtyah%26trkInfo%3Dtas%253AFORTRESS%2520MEDICAL%252Cidx%253A1-2-2&secure%5Burl_type%5D=linkedin_company_website)  
8 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 67% Medium, 33% Large

#### What Are Recent G2 Reviews of Clindex?

**["A wonderful system to work in"](https://www.g2.com/survey_responses/clindex-review-714681)**

**Rating:** 4.5/5.0 stars

_— Cynthia K._

[Read full review](https://www.g2.com/survey_responses/clindex-review-714681)

**["Easy CTMS Implementation and Smooth Integration with Marvin EDC"](https://www.g2.com/survey_responses/clindex-review-12579360)**

**Rating:** 4.5/5.0 stars

_— Verified User in Information Technology and Services_

[Read full review](https://www.g2.com/survey_responses/clindex-review-12579360)

[
Clinevo eTMF
](https://www.g2.com/products/clinevo-etmf/reviews)

By [Clinevo Technologies](https://www.g2.com/sellers/clinevo-technologies)

[

0/5(0)

](https://www.g2.com/products/clinevo-etmf/reviews)

Product Description

We are a Software Development Company specialized in developing and implementing robust technology solutions for Life Sciences R&D. We help Pharma, Biotech and CROs in reducing their time and cost

### [Clinevo eTMF](https://www.g2.com/products/clinevo-etmf/reviews)

We are a Software Development Company specialized in developing and implementing robust technology solutions for Life Sciences R&D. We help Pharma, Biotech and CROs in reducing their time and cost in Clinical trials by implementing innovative technologies that involves Data warehousing, Analytics, Collaboration, Automation, and Artificial Intelligence. We are committed towards delivering the most efficient and practical end-to-end solutions with HIPAA, GXP, CSV, 21 CFR Part 11 and other applicable regulatory guidelines. Our unmatched domain experience and technology expertise enable us to deliver the best solutions.

#### Who Is the Company Behind Clinevo eTMF?

- **Seller:** [Clinevo Technologies](https://www.g2.com/sellers/clinevo-technologies)
- **Year Founded:** 2016
- **HQ Location:** Bangalore, IN
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=3604b5075db182e4c17e9602441fda9b14b5c1ca481818a1d90c2b86a6d621f2&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F13426084&secure%5Burl_type%5D=linkedin_company_website)  
98 employees on LinkedIn®

[
ClinicalHawk eTMF
](https://www.g2.com/products/clinicalhawk-etmf/reviews)

By [N2NAcers](https://www.g2.com/sellers/n2nacers)

[

0/5(0)

](https://www.g2.com/products/clinicalhawk-etmf/reviews)

Product Description

Our electronic Trial Master File (eTMF) simplifies today’s over-engineered products and implementations by empowering oversight without busting the budget. ClinicalHawk eTMF software is one of its kin

### [ClinicalHawk eTMF](https://www.g2.com/products/clinicalhawk-etmf/reviews)

Our electronic Trial Master File (eTMF) simplifies today’s over-engineered products and implementations by empowering oversight without busting the budget. ClinicalHawk eTMF software is one of its kind for managing documents in real-time as the TMF is generated to ensure a constant state of inspection readiness, increase visibility oversight, and improve collaboration.

#### Who Is the Company Behind ClinicalHawk eTMF?

- **Seller:** [N2NAcers](https://www.g2.com/sellers/n2nacers)
- **Year Founded:** 2021
- **HQ Location:** Ahmedabad, IN
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=e590951d7cbd6bc248f9e0f405ddc8b4485a582da699f106fe5a1f460c867881&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fclinicalhawk&secure%5Burl_type%5D=linkedin_company_website)  
2 employees on LinkedIn®

[
Clinion
](https://www.g2.com/products/clinion/reviews)

By [Clinion](https://www.g2.com/sellers/clinion-e18ccd88-cb44-4bcb-a5cf-8a814664dc7a)

[

4.5/5(3)

](https://www.g2.com/products/clinion/reviews)

Product Description

Clinion’s AI-enabled eClinical platform offers a unified suite of solutions - EDC, RTSM, CTMS, eConsent, ePRO, eSource, eProtocol Automation, CSR Automation, and eTMF, driving efficiency and ensuring

### [Clinion](https://www.g2.com/products/clinion/reviews)

Clinion’s AI-enabled eClinical platform offers a unified suite of solutions - EDC, RTSM, CTMS, eConsent, ePRO, eSource, eProtocol Automation, CSR Automation, and eTMF, driving efficiency and ensuring continuity across all stages of a clinical trial. Clinion enables users to effortlessly manage the complexities of clinical trials by sharing consistent trial data across the entire trial process leading to accelerated clinical development, increased compliance, and faster go-to-market. Key Differentiators ● Accelerated Study Setup From protocol to production, Clinion enables rapid study builds using standardized libraries and reusable components. ● Deeply Embedded AI Across Workflows AI supports protocol generation, edit check creation, medical coding, and data review, reducing manual effort at every stage. ● Agentic AI for Data Review Context-aware AI reads protocol and CRF together to flag relevant issues and reduce unnecessary queries. ● Faster Database Lock with Better Data Quality Automated validations and AI-assisted review help resolve discrepancies earlier and shorten study timelines. ● Unified Platform with Shared Trial Data EDC, RTSM, CTMS, eConsent, ePRO, eSource, eProtocol Automation, and CSR Automation operate on a single data layer, reducing reconciliation effort and improving consistency. ● Intuitive System with Minimal Training Clean interface and logical workflows make it easy for sites and sponsors to get started quickly. ● Predictable and Transparent Pricing Flat subscription model with no hidden costs, suitable for both short-term and long-duration studies.

**Average Rating:** 4.5/5.0

**Total Reviews:** 2

#### How Do G2 Users Rate Clinion?

- **Ease of Use:** 9.2/10 (Category avg: 8.9/10)
- **Quality of Support:** 10.0/10 (Category avg: 8.3/10)

#### Who Is the Company Behind Clinion?

- **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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=80a4b4cfcd2079ae61cb49a8f235d240e281e57076225a15d0e5da44c573d264&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fclinion-eclinical-platform%2F%3FviewAsMember%3Dtrue&secure%5Burl_type%5D=linkedin_company_website)  
64 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 100% Small

#### What Are Recent G2 Reviews of Clinion?

**["A good platform for AI based for e-clinical trials!"](https://www.g2.com/survey_responses/clinion-review-7334649)**

**Rating:** 4.0/5.0 stars

_— Aryavatta S._

[Read full review](https://www.g2.com/survey_responses/clinion-review-7334649)

**["GREAT SOFTWARE FOR ELECTRONIC DATA CAPTURING."](https://www.g2.com/survey_responses/clinion-review-7358031)**

**Rating:** 5.0/5.0 stars

_— Riya M._

[Read full review](https://www.g2.com/survey_responses/clinion-review-7358031)

#### What Are G2 Users Discussing About Clinion?

- [What is Clinion used for?](https://www.g2.com/discussions/what-is-clinion-used-for)

[
Clinion eTMF
](https://www.g2.com/products/clinion-etmf/reviews)

By [Clinion](https://www.g2.com/sellers/clinion-e18ccd88-cb44-4bcb-a5cf-8a814664dc7a)

[

0/5(0)

](https://www.g2.com/products/clinion-etmf/reviews)

Product Description

Clinion eTMF helps the team manage clinical trial documents in a structured way, with real-time tracking and consistent oversight. It reduces the need for manual follow-ups and keeps documentation ali

### [Clinion eTMF](https://www.g2.com/products/clinion-etmf/reviews)

Clinion eTMF helps the team manage clinical trial documents in a structured way, with real-time tracking and consistent oversight. It reduces the need for manual follow-ups and keeps documentation aligned with study requirements throughout the trial. What can you expect? ● Defined TMF Structure Set up file plans using standard or custom structures across study, country, and site levels. ● Real-Time Tracking of Documents Track expected documents and identify missing or delayed files as the study progresses. ● Controlled Review and Approval Manage document workflows with review, QC, and approval steps, including e-signatures. ● Ongoing Visibility Monitor completeness and status through dashboards without waiting for end-of-study checks. ● Flexible Configuration Adapt the TMF structure and workflows based on study or sponsor requirements. ● Audit-Ready Records Maintain version history and activity logs to support inspections and compliance. Impact Reduced reconciliation effort during closeout Lower manual tracking effort Better visibility into document status

#### Who Is the Company Behind Clinion eTMF?

- **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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=80a4b4cfcd2079ae61cb49a8f235d240e281e57076225a15d0e5da44c573d264&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fclinion-eclinical-platform%2F%3FviewAsMember%3Dtrue&secure%5Burl_type%5D=linkedin_company_website)  
64 employees on LinkedIn®

[
ClinVigilant eClinical
](https://www.g2.com/products/clinvigilant-eclinical/reviews)

By [ClinVigilant](https://www.g2.com/sellers/clinvigilant)

[

0/5(0)

](https://www.g2.com/products/clinvigilant-eclinical/reviews)

Product Description

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-market

### [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:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=f5cec8d75a4360da6855cb428b870ff577cef7e3f22c0f20910eb33a1a8bc88d&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fclinvigilantresearch&secure%5Burl_type%5D=linkedin_company_website)  
19 employees on LinkedIn®

[
Cloudbyz eTMF
](https://www.g2.com/products/cloudbyz-etmf/reviews)

By [Cloudbyz](https://www.g2.com/sellers/cloudbyz)

[

0/5(0)

](https://www.g2.com/products/cloudbyz-etmf/reviews)

Product Description

Cloudbyz eTMF solution offers a cloud-based repository of all clinical trial documents including files, images, information, etc. Digitally store, manage, and share all clinical trial-related document

### [Cloudbyz eTMF](https://www.g2.com/products/cloudbyz-etmf/reviews)

Cloudbyz eTMF solution offers a cloud-based repository of all clinical trial documents including files, images, information, etc. Digitally store, manage, and share all clinical trial-related documents with a centralized overview. Manage essential trial documents, stay inspection ready, and enable real-time visibility for CROs, sponsors, monitors, and other stakeholders in a clinical trial.

#### Who Is the Company Behind Cloudbyz eTMF?

- **Seller:** [Cloudbyz](https://www.g2.com/sellers/cloudbyz)
- **Year Founded:** 2014
- **HQ Location:** Naperville, US
- **Twitter:** @cloudbyz  
399 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=e57128dc3532a199487bcdf18555bba6ab729b9e9f8407a6280ea904853836af&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fcloudbyz&secure%5Burl_type%5D=linkedin_company_website)  
100 employees on LinkedIn®

[
ComplyDocs eTMF
](https://www.g2.com/products/complydocs-etmf/reviews)

By [ComplyDocs](https://www.g2.com/sellers/complydocs)

[

0/5(0)

](https://www.g2.com/products/complydocs-etmf/reviews)

Product Description

ComplyDocs eTMF is an electronic Trial Master File (eTMF solution designed to digitize and streamline the management of essential clinical trial documents. By transitioning from traditional paper-base

### [ComplyDocs eTMF](https://www.g2.com/products/complydocs-etmf/reviews)

ComplyDocs eTMF is an electronic Trial Master File (eTMF solution designed to digitize and streamline the management of essential clinical trial documents. By transitioning from traditional paper-based systems to a digital platform, ComplyDocs eTMF enhances the efficiency, accessibility, and compliance of clinical trial documentation processes. Key Features and Functionality: - Digital Document Management: Enables the electronic capture, organization, and storage of all essential clinical trial documents, ensuring centralized access and improved document control. - Regulatory Compliance: Supports adherence to regulatory requirements by maintaining comprehensive audit trails, version control, and secure access, aligning with standards such as FDA 21 CFR Part 11. - Collaboration Tools: Facilitates seamless collaboration among clinical trial stakeholders through user-friendly interfaces and robust functionalities, allowing for efficient document sharing and communication. - Automated Workflows: Streamlines processes with automated workflows for document review, approval, and archiving, reducing manual tasks and minimizing errors. - Real-Time Monitoring: Provides real-time tracking and reporting capabilities, offering insights into document status and trial progress to ensure timely decision-making. Primary Value and User Solutions: ComplyDocs eTMF addresses the challenges associated with managing vast amounts of clinical trial documentation by offering a centralized, digital solution that enhances efficiency and compliance. It reduces the reliance on paper-based systems, minimizes the risk of document mismanagement, and ensures that all trial documents are audit-ready and easily accessible. By automating workflows and facilitating collaboration, ComplyDocs eTMF helps organizations accelerate trial timelines, maintain regulatory compliance, and improve overall trial management.

#### Who Is the Company Behind ComplyDocs eTMF?

- **Seller:** [ComplyDocs](https://www.g2.com/sellers/complydocs)
- **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®

[
ConciergeTMF
](https://www.g2.com/products/conciergetmf/reviews)

By [ConciergeTMF](https://www.g2.com/sellers/conciergetmf)

[

0/5(0)

](https://www.g2.com/products/conciergetmf/reviews)

Product Description

ConciergeTMF is an innovative Software-as-a-Service (SaaS) provider specializing in Research and Development (R&D) archival management. Their unique approach transcends traditional software soluti

### [ConciergeTMF](https://www.g2.com/products/conciergetmf/reviews)

ConciergeTMF is an innovative Software-as-a-Service (SaaS) provider specializing in Research and Development (R&D) archival management. Their unique approach transcends traditional software solutions by offering a comprehensive platform that seamlessly blends technology and human expertise. Key features of ConciergeTMF's platform include: Human-in-the-Loop Intelligence: At the core of ConciergeTMF's offering is the fusion of AI technology with human oversight. This synergy ensures that document management is not only efficient but also exceptionally precise, reliable, and trustworthy. Dynamic Event Center: The platform boasts a Dynamic Event Center that provides real-time visibility into document progress. It facilitates storyboarding and offers gamified project management tools, empowering users with a holistic view of their document journeys. Multi-Channel and Passive Access Communications: ConciergeTMF simplifies communication by offering a unified platform for email, text routing, and task location placeholders. This feature promotes effortless collaboration and coordination among team members, enhancing productivity. Streamlined Processes: With ConciergeTMF, users bid farewell to repetitive tasks such as uploading and redundant user administration. The platform streamlines document workflows and eliminates access management hassles, allowing teams to focus on high-impact activities. End-to-End TMF Platform: ConciergeTMF's platform is designed to facilitate end-to-end document retention. It ensures agility in a dynamic research landscape, providing the flexibility and compliance needed in the field. ConciergeTMF's commitment to excellence is evident in their comprehensive approach to R&D archival management. By seamlessly integrating technology with human intelligence, they empower organizations to achieve unmatched precision, efficiency, and compliance in their document management processes. Experience the transformative power of ConciergeTMF's SaaS platform and unlock the full potential of your R&D archival management.

#### Who Is the Company Behind ConciergeTMF?

- **Seller:** [ConciergeTMF](https://www.g2.com/sellers/conciergetmf)
- **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®

[
CREx Software
](https://www.g2.com/products/crex-software/reviews)

By [CREx Software](https://www.g2.com/sellers/crex-software)

[

0/5(0)

](https://www.g2.com/products/crex-software/reviews)

Product Description

CREx is a commercial real estate data platform and managed data service for owners, asset managers, and investors who need clean, governed data. CREx OS integrates with Yardi, AppFolio, Entrata, MRI

### [CREx Software](https://www.g2.com/products/crex-software/reviews)

CREx is a commercial real estate data platform and managed data service for owners, asset managers, and investors who need clean, governed data. CREx OS integrates with Yardi, AppFolio, Entrata, MRI, and RealPage. It automates the feeds, reconciles charts of accounts across PM systems, versions every snapshot for audit, and controls access by property and report. Governance sits in the data layer, not in a policy document. The models sit on top. Loan and covenant tracking against actual performance. Twelve-month forecasts built from your trailing actuals. Property-level performance scoring against portfolio and market benchmarks. Every dataset is exposed through an MCP server, so Claude and other AI tools query your live portfolio on day one. No integration project. CREx also staffs the work. Our fractional asset management team is AI-native and forward-deployed inside your monthly reporting cycle.

#### Who Is the Company Behind CREx Software?

- **Seller:** [CREx Software](https://www.g2.com/sellers/crex-software)
- **Year Founded:** 2021
- **HQ Location:** New York, US
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=79ecd7417924308788f4836bf90d7f2ac815fb9fac23a664e3be2deb174edfb8&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F74115963&secure%5Burl_type%5D=linkedin_company_website)  
25 employees on LinkedIn®

[
Ennov Clinical
](https://www.g2.com/products/ennov-clinical/reviews)

By [Ennov](https://www.g2.com/sellers/ennov)

[

4.5/5(1)

](https://www.g2.com/products/ennov-clinical/reviews)

Product Description

Ennov Clinical Software Suite is an end-to-end solution for managing all aspects of clinical trials, from planning through execution and close-out. Designed for sponsors, CROs, investigators, and

### [Ennov Clinical](https://www.g2.com/products/ennov-clinical/reviews)

Ennov Clinical Software Suite is an end-to-end solution for managing all aspects of clinical trials, from planning through execution and close-out. Designed for sponsors, CROs, investigators, and patients, the suite integrates clinical data management and trial management into a single platform. It includes Ennov EDC, RTSM, ePRO, CTMS, and eTMF, offering seamless deployment in the cloud or on premises. This comprehensive suite improves trial efficiency by centralizing data, automating processes, and enhancing collaboration across global teams. With real-time visibility and robust reporting, Ennov Clinical ensures compliance with industry standards while reducing costs and improving decision-making. The suite’s eLearning application further enhances user proficiency, making it a complete solution for modern clinical trials.

**Average Rating:** 4.5/5.0

**Total Reviews:** 1

#### How Do G2 Users Rate Ennov Clinical?

- **Ease of Use:** 10.0/10 (Category avg: 8.9/10)
- **Quality of Support:** 10.0/10 (Category avg: 8.3/10)

#### Who Is the Company Behind Ennov Clinical?

- **Seller:** [Ennov](https://www.g2.com/sellers/ennov)
- **Year Founded:** 1999
- **HQ Location:** Paris, FR
- **Twitter:** @EnnovGroup  
889 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=b213021976e02cf2525be25f895b3248b00aa1b72645beb4bec6167ff4c531f6&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F81570&secure%5Burl_type%5D=linkedin_company_website)  
304 employees on LinkedIn®
- **Ownership:** Private

#### Who Uses This Product?

- **Company Size:** 100% Medium

#### What Are Recent G2 Reviews of Ennov Clinical?

**["Good Software to manage large sample clinical trials"](https://www.g2.com/survey_responses/ennov-clinical-review-8280353)**

**Rating:** 4.5/5.0 stars

_— Anand P._

[Read full review](https://www.g2.com/survey_responses/ennov-clinical-review-8280353)

[
eTMF Connect
](https://www.g2.com/products/etmf-connect/reviews)

By [Montrium](https://www.g2.com/sellers/montrium)

[

0/5(0)

](https://www.g2.com/products/etmf-connect/reviews)

Product Description

Key Features and Functionality: eTMF Connect is cloud-based electronic Trial Master File (eTMF) management software designed for clinical operations teams managing multiple studies. The system automa

### [eTMF Connect](https://www.g2.com/products/etmf-connect/reviews)

Key Features and Functionality: eTMF Connect is cloud-based electronic Trial Master File (eTMF) management software designed for clinical operations teams managing multiple studies. The system automates trial documentation workflows while providing real-time visibility into TMF completeness and inspection readiness. Document Management: - eTMF Navigator: Interactive dashboard displaying TMF completeness at study, country, and site levels with visual indicators for missing documents - TMF Reference Model Alignment: Pre-configured study structures aligned to the latest TMF Reference Model - Placeholder Management: Generates expected document placeholders before documents exist, enabling visibility into what's missing vs. what's filed - Document Template Center: Centralized library of standardized document templates to accelerate creation and ensure consistency - Version Control: Automatic versioning with full audit trails tracking all document changes and approvals Workflow Automation: - Clinical Inbox: Sites email documents to study-specific addresses; documents automatically queue in staging area for review - Configurable QC Workflows: Multi-step review and approval processes with automated task assignments and reminders - Drag-and-Drop Filing: Direct filing by dragging documents onto placeholders in the Navigator - Task Center: Centralized location to view and complete all document-related tasks with filtering options Collaboration and Access: - Role-Based Access Control: Scoped permissions by study, country, or site ensure users see only relevant content - Inspector Access: Dedicated read-only access mode for regulators during inspections - External Contributor Support: Sites and CROs participate without requiring full system accounts - Blinding Process Management: Support for blinded studies with controlled access to unblinded documents Search and Reporting: - Advanced Search: Google-like search with metadata filtering and TMF Reference Model zone filtering - Real-time Reporting: Completeness dashboards, timeliness metrics, and quality KPIs update automatically - Excel Export: Export TMF data for advanced analysis - Comprehensive Audit Trails: Track all document activity for regulatory inspections - Timeliness Reports: Excel reports showing KPI performance metrics - Rejected Documents Report: View all rejected documents and rejection reasons Compliance: 21 CFR Part 11 and EudraLex Annex 11 compliant, hosted on Microsoft Azure with SOC 2 Type I certification, GDPR compliant data handling. Problems solved: Organizations transitioning from paper-based, SharePoint, or file-sharing TMF systems face inspection readiness anxiety from lack of real-time completeness visibility, scaling constraints as manual processes don't support multiple studies across sites, administrative overhead from repetitive filing and indexing work, and collaboration barriers managing documentation from distributed teams. Value delivered: - Continuous inspection readiness: eTMF Navigator provides instant visual overview of TMF completeness, identifying missing documents immediately - Operational efficiency: Clinical inbox and staging area capabilities reduce administrative burden from document collection and processing - Accelerated study startup: Pre-configured TMF structures eliminate repetitive setup work - Simplified collaboration: Sites email documents without system accounts; role-based access ensures stakeholders see only relevant content - Rapid implementation: 3-8 week timeline with included validation package - Remote team enablement: Cloud-based access allows distributed teams to collaborate from any location Target users: TMF Managers, Clinical Operations Managers, Document Specialists, Regulatory Affairs professionals, and QA teams at biotech, pharma, and CRO organizations managing clinical trials.

#### Who Is the Company Behind eTMF Connect?

- **Seller:** [Montrium](https://www.g2.com/sellers/montrium)
- **Year Founded:** 2005
- **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=26f03ab6572a376d540de9371a6184f4adfcd28fd6899ba13b5abb817d69a106&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fmontrium&secure%5Burl_type%5D=linkedin_company_website)  
56 employees on LinkedIn®

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

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

[Browse Electronic Trial Master File (eTMF) Themes](/categories/electronic-trial-master-file-etmf/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

Electronic trial master file (eTMF) software is a specialized content management system that captures, stores, and manages all essential documents and images from a clinical trial. These solutions speed up content management via templates, mobile scanning, document classification, AI-powered automation, and approval workflows.

Organizations such as pharmaceutical and biotech companies that conduct regulated clinical trials need to maintain a TMF to comply with government regulatory requirements. By digitizing essential trial documents and content, an eTMF offers greater quality control and visibility over processes and documentation, making it easier to audit content throughout the trial lifecycle to ensure compliance is being met. Sites, sponsors, and contract research organizations (CROs) can collaborate in real-time on the TMF, track key metrics for study completion, share and migrate content, and search and filter data.

An eTMF supports [clinical trial management software](https://www.g2.com/categories/clinical-trial-management) and [electronic data capture (EDC) software](https://www.g2.com/categories/electronic-data-capture-edc) by importing documents from both solutions, as well as automating the creation and filing of new documents using information stored in both.

To qualify for inclusion in the Electronic Trial Master File (eTMF) category, a product must:

- Provide pre-built and customizable TMF reference models, and allow specifications to be configured at the study, country, and site levels
- Track the status of all necessary trial documents from missing to completed stages and provide analytics
- Establish review and approval workflows
- Allow document authoring and collaboration between internal and external parties
- Comply with all relevant government regulatory requirements for clinical trials, such as 21 CFR Part 11, HIPAA, ANNEX 11, GxP, and GDPR

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