# Best Electronic Data Capture (EDC) Software - Page 3

*By [Emma Stein](https://research.g2.com/insights/author/emma-stein)*


Electronic data capture (EDC) software replaces the traditional and very manual process of managing clinical trial data with an electronic system. At its core, EDC software streamlines the collection, review, and processing of clinical trial data. [Clinical trial management software](https://www.g2.com/categories/clinical-trial-management) is bolstered by EDC software; some even offer EDC functionality within the CTMS. Benefits of using EDC software include improved data quality and study efficiency, as well as an improved ability to meet regulatory compliance. Contract research organizations (CROs), clinical trial sponsors, and study sites all utilize EDC software.

To qualify for inclusion in the EDC category, a product must:

- Capture and store clinical trial data
- Simplify the process of sharing and exporting of data
- Enforce querying of stored clinical trial data






## G2 Grid® for Electronic Data Capture (EDC) Software
![G2 Grid® for Electronic Data Capture (EDC) Software plotting products by satisfaction and market presence](https://www.g2.com/categories/electronic-data-capture-edc/grids.png?focus%5B%5D=1366872&focus%5B%5D=51250&focus%5B%5D=94249&focus%5B%5D=90824&focus%5B%5D=44344&focus%5B%5D=128837&focus%5B%5D=26533&focus%5B%5D=43817)
Highlighted products: cubeCDMS, Medrio EDC, Viedoc, Medidata Rave, Greenlight Guru Clinical, Oracle Clinical, Castor, and iMednet EDC.
Underlying data: [Grid® JSON](https://www.g2.com/categories/electronic-data-capture-edc/grids.json?focus%5B%5D=cubecdms&amp;focus%5B%5D=medrio-edc&amp;focus%5B%5D=viedoc&amp;focus%5B%5D=medidata-rave&amp;focus%5B%5D=greenlight-guru-clinical&amp;focus%5B%5D=oracle-clinical&amp;focus%5B%5D=castor-edc-castor&amp;focus%5B%5D=imednet-edc)


## How Many Electronic Data Capture (EDC) Software Products Does G2 Track?
**Total Products under this Category:** 116

### Category Stats (Jul 2026)
- **Average Rating**: 4.27/5 The average rating of products in this category, based on all submitted ratings
- **Top Trending Product**: cubeCDMS (+1.05%) - Among all products in this category, cubeCDMS recorded the largest rating increase compared to last month
*Last updated: July 16, 2026*


## How Does G2 Rank Electronic Data Capture (EDC) Software Products?

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

- 30 Analysts and Data Experts
- 1,700+ Authentic Reviews
- 116+ 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 Electronic Data Capture (EDC) Software Is Best for Your Use Case?

- **Leader:** [cubeCDMS](https://www.g2.com/products/cubecdms/reviews)
- **Highest Performer:** [Prelude EDC](https://www.g2.com/products/prelude-edc/reviews)
- **Easiest to Use:** [cubeCDMS](https://www.g2.com/products/cubecdms/reviews)
- **Top Trending:** [cubeCDMS](https://www.g2.com/products/cubecdms/reviews)
- **Best Free Software:** [Viedoc](https://www.g2.com/products/viedoc/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&amp;secure%5Bad_slot%5D=category_product_list&amp;secure%5Bcategory_id%5D=1733&amp;secure%5Bchosen_at%5D=2026-07-16T09%3A49%3A04Z&amp;secure%5Bdisplayable_resource_id%5D=1733&amp;secure%5Bdisplayable_resource_type%5D=Category&amp;secure%5Bmedium%5D=sponsored&amp;secure%5Bplacement_reason%5D=page_category&amp;secure%5Bplacement_resource_ids%5D%5B%5D=1733&amp;secure%5Bprioritized%5D=false&amp;secure%5Bproduct_id%5D=1870742&amp;secure%5Bresource_id%5D=1733&amp;secure%5Bresource_type%5D=Category&amp;secure%5Bsource_type%5D=category_page&amp;secure%5Bsource_url%5D=https%3A%2F%2Fwww.g2.com%2Fcategories%2Felectronic-data-capture-edc%3Fopen_modal_url%3D%252Fproducts%252Fredcap%252Fwishlists%253Fhost_path%253D%25252Fcategories%25252Felectronic-data-capture-edc%2526source%253Dcategory&amp;secure%5Btoken%5D=0986de90e8cc9766ce77011b5ff518d058d38158cbfef50a388fb42f712b7e4e&amp;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&amp;secure%5Burl_type%5D=custom_url)

---

## What Are the Top-Rated Electronic Data Capture (EDC) Software Products in 2026?
### 1. [Med-Quest](https://www.g2.com/products/med-quest/reviews)
Med-Quests unique approach to collecting data means serious time savings for you and your team.


**Average Rating:** 4.5/5.0
**Total Reviews:** 1
**How Do G2 Users Rate Med-Quest?**

- **Quality of Support:** 10.0/10 (Category avg: 8.7/10)

**Who Is the Company Behind Med-Quest?**

- **Seller:** [Med-Quest](https://www.g2.com/sellers/med-quest)
- **HQ Location:** N/A
- **LinkedIn® Page:** https://www.linkedin.com/company/No-Linkedin-Presence-Added-Intentionally-By-DataOps (1 employees on LinkedIn®)

**Who Uses This Product?**
- **Company Size:** 100% Mid-Market



#### What Are Recent G2 Reviews of Med-Quest?

**"[Med-Quest](https://www.g2.com/survey_responses/med-quest-review-10060210)"**

**Rating:** 4.5/5.0 stars
*— Frank C.*

[Read full review](https://www.g2.com/survey_responses/med-quest-review-10060210)

---



### 2. [PerkinElmer Signals Screening](https://www.g2.com/products/perkinelmer-signals-screening/reviews)
Signals Screening is an intuitive, configurable, and flexible screening workflow processing engine on top of the unparalleled data visualization and analysis capabilities of TIBCO Spotfire.


**Average Rating:** 4.5/5.0
**Total Reviews:** 1
**How Do G2 Users Rate PerkinElmer Signals Screening?**

- **Data Capture - Electronic Data Capture (EDC):** 8.3/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 8.3/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 8.3/10 (Category avg: 8.8/10)
- **Quality of Support:** 8.3/10 (Category avg: 8.7/10)

**Who Is the Company Behind PerkinElmer Signals Screening?**

- **Seller:** [Indica Labs Company](https://www.g2.com/sellers/indica-labs-company)
- **Year Founded:** 2011
- **HQ Location:** Albuquerque, New Mexico, United States
- **Twitter:** @Indica_Labs (937 Twitter followers)
- **LinkedIn® Page:** https://www.linkedin.com/company/indica-labs (117 employees on LinkedIn®)

**Who Uses This Product?**
- **Company Size:** 100% Enterprise



#### What Are Recent G2 Reviews of PerkinElmer Signals Screening?

**"[Perkin elmer signals](https://www.g2.com/survey_responses/perkinelmer-signals-screening-review-8926144)"**

**Rating:** 4.5/5.0 stars
*— Verified User in Health, Wellness and Fitness*

[Read full review](https://www.g2.com/survey_responses/perkinelmer-signals-screening-review-8926144)

---



### 3. [QuesGen EDC](https://www.g2.com/products/quesgen-edc/reviews)
A web-based solution that can be used for recruiting patients and managing all aspects of data associated with clinical research.


**Average Rating:** 4.5/5.0
**Total Reviews:** 1
**How Do G2 Users Rate QuesGen EDC?**

- **Data Capture - Electronic Data Capture (EDC):** 10.0/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 8.3/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 8.3/10 (Category avg: 8.8/10)
- **Quality of Support:** 8.3/10 (Category avg: 8.7/10)

**Who Is the Company Behind QuesGen EDC?**

- **Seller:** [QuesGen Systems](https://www.g2.com/sellers/quesgen-systems)
- **Year Founded:** 2004
- **HQ Location:** San Mateo, US
- **LinkedIn® Page:** https://www.linkedin.com/company/299889 (10 employees on LinkedIn®)

**Who Uses This Product?**
- **Company Size:** 100% Enterprise



#### What Are Recent G2 Reviews of QuesGen EDC?

**"[Great Platform for clinical management](https://www.g2.com/survey_responses/quesgen-edc-review-7388548)"**

**Rating:** 4.5/5.0 stars
*— Daleep K.*

[Read full review](https://www.g2.com/survey_responses/quesgen-edc-review-7388548)

---



### 4. [SyMetric](https://www.g2.com/products/symetric/reviews)
SyMetric offers cloud-based, end-to-end solutions for Clinical Research, from Manufacturing to the Submissions. The Product suit is built as an ERP, on a single database providing a seamless flow of data across modules. Products: 1. SyMetric Clinical Trial Platform SyMetric Integrated Cloud-Based Clinical Trial Platform is fully modularized, allowing you to choose the right solution that can be configured to suit your trial requirements. You can plan, monitor, and manage trials effectively, every step of the way. Designed, developed, and deployed by us, our all-encompassing set of solutions that is IRT/IWRS, EDC, Medical Coding, CTM, and Trial Analytics on a single database built to work seamlessly with your existing ecosystem and processes. It covers various processes in Clinical Trials – including Study Master Management, Subject Management, Clinical Supplies Management, Data Management, and Medical Coding. With SyMetric Clinical Trial Platform, you can manage, monitor, analyze, and report with ease by configuring the solutions to your specific needs – whether you are a Pharmaceutical Sponsor, Clinical Research Organization (CRO), or from the Academia. 2. SyMetric Trial Analytics The SyMetric Trial Analytics solution helps you make informed decisions while planning a new Clinical Trial using insights from historic study data and performance analytics of stakeholders such as CROs, Investigation Sites, and Investigators. With our Analytics Tool, you can cut Trial Planning time significantly and enhance efficiency. Also, the system is built on the SAP Business Technology Platform, enabling you to explore various services that SAP has to offer in the Cloud. Our solution can be integrated with your system to deliver insightful analysis while leveraging cloud initiatives from SAP in Life Sciences. Here are the various sources of data that we analyze to help you plan effectively.


**Average Rating:** 5.0/5.0
**Total Reviews:** 1

**Who Is the Company Behind SyMetric?**

- **Seller:** [SyMetric Systems](https://www.g2.com/sellers/symetric-systems)
- **Year Founded:** 2012
- **HQ Location:** Bengaluru, IN
- **LinkedIn® Page:** https://www.linkedin.com/company/symetric-systems/ (38 employees on LinkedIn®)

**Who Uses This Product?**
- **Company Size:** 100% Enterprise



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

**"[It is a a experience as I have been getting hang  things](https://www.g2.com/survey_responses/symetric-review-7147186)"**

**Rating:** 5.0/5.0 stars
*— Thando M.*

[Read full review](https://www.g2.com/survey_responses/symetric-review-7147186)

---



### 5. [The Observer XT](https://www.g2.com/products/the-observer-xt/reviews)
The Observer XT is the professional and user-friendly software package for the collection, analysis, and presentation of observational data.


**Average Rating:** 1.5/5.0
**Total Reviews:** 1
**How Do G2 Users Rate The Observer XT?**

- **Quality of Support:** 0.0/10 (Category avg: 8.7/10)

**Who Is the Company Behind The Observer XT?**

- **Seller:** [Noldus Information Technology](https://www.g2.com/sellers/noldus-information-technology)
- **Year Founded:** 1989
- **HQ Location:** Wageningen, NL
- **Twitter:** @NoldusIT (2,002 Twitter followers)
- **LinkedIn® Page:** https://www.linkedin.com/company/noldus-information-technology (151 employees on LinkedIn®)

**Who Uses This Product?**
- **Company Size:** 100% Small-Business




#### What Are G2 Users Discussing About The Observer XT?

- [What is The Observer XT used for?](https://www.g2.com/discussions/what-is-the-observer-xt-used-for)

### 6. [TIBCO Cloud Integration (SaaS)](https://www.g2.com/products/tibco-cloud-integration-saas/reviews)
TIBCO Cloud Integration is a versatile integration Platform as a Service (iPaaS designed to help businesses seamlessly connect applications, data sources, and devices across on-premises and cloud environments. Its intuitive, no-code interface enables users—from business analysts to developers—to create, test, and deploy integrations swiftly, enhancing operational efficiency and agility. Key Features and Functionality: - No-Code Development: Empowers users to design integration workflows without coding, utilizing a drag-and-drop visual interface. - Pre-Built Connectors: Offers a wide array of connectors for popular SaaS applications like Salesforce, ServiceNow, and Workday, facilitating quick integrations. - API Management: Allows for the creation, publication, and management of APIs, supporting various specifications such as OpenAPI, gRPC, GraphQL, and AsyncAPI. - Event-Driven Architecture: Supports real-time data processing and event-based workflows, enabling responsive application behavior. - Flexible Deployment: Supports deployment across containers, on-premises, cloud, serverless environments, and edge devices, providing scalability and adaptability. - Robust Security: Implements comprehensive security measures, including authentication, authorization, and encryption, to protect data integrity. Primary Value and User Solutions: TIBCO Cloud Integration addresses the challenge of connecting disparate systems and applications within an organization. By providing a user-friendly, no-code platform with extensive pre-built connectors and flexible deployment options, it enables businesses to: - Accelerate Integration Processes: Reduce the time and effort required to integrate various applications and data sources. - Enhance Business Agility: Quickly adapt to changing business needs by enabling users to create and modify integrations without extensive technical expertise. - Improve Operational Efficiency: Automate workflows and data synchronization, reducing manual tasks and minimizing errors. - Ensure Scalability and Security: Deploy integrations across diverse environments securely, supporting growth and compliance requirements. By streamlining the integration process, TIBCO Cloud Integration empowers organizations to focus on innovation and delivering value to their customers.


**Average Rating:** 2.5/5.0
**Total Reviews:** 1
**How Do G2 Users Rate TIBCO Cloud Integration (SaaS)?**

- **Data Capture - Electronic Data Capture (EDC):** 6.7/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 3.3/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 3.3/10 (Category avg: 8.8/10)
- **Quality of Support:** 5.0/10 (Category avg: 8.7/10)

**Who Is the Company Behind TIBCO Cloud Integration (SaaS)?**

- **Seller:** [Cloud Software Group](https://www.g2.com/sellers/cloud-software-group)
- **HQ Location:** Fort Lauderdale, FL
- **Twitter:** @cloudsoftware (124 Twitter followers)
- **LinkedIn® Page:** https://www.linkedin.com/company/cloudsoftwaregroup/ (9,527 employees on LinkedIn®)

**Who Uses This Product?**
- **Company Size:** 100% Enterprise





### 7. [YPrime eCOA](https://www.g2.com/products/yprime-ecoa/reviews)
YPrimes eCOA platform for patient data collection is fundamentally different than what any other providers in the industry can offer. The first and only application-based eCOA platform gives unprecedented flexibility, speed &amp; precision for your study needs.


**Average Rating:** 4.5/5.0
**Total Reviews:** 1
**How Do G2 Users Rate YPrime eCOA?**

- **Quality of Support:** 8.3/10 (Category avg: 8.7/10)

**Who Is the Company Behind YPrime eCOA?**

- **Seller:** [YPrime](https://www.g2.com/sellers/yprime)
- **Year Founded:** 2006
- **HQ Location:** Malvern, US
- **Twitter:** @Y_Prime (367 Twitter followers)
- **LinkedIn® Page:** https://www.linkedin.com/company/y-prime/ (308 employees on LinkedIn®)

**Who Uses This Product?**
- **Company Size:** 100% Small-Business



#### What Are Recent G2 Reviews of YPrime eCOA?

**"[YPrime COA](https://www.g2.com/survey_responses/yprime-ecoa-review-3379379)"**

**Rating:** 4.5/5.0 stars
*— Verified User in Research*

[Read full review](https://www.g2.com/survey_responses/yprime-ecoa-review-3379379)

---


#### What Are G2 Users Discussing About YPrime eCOA?

- [What is YPrime eCOA used for?](https://www.g2.com/discussions/what-is-yprime-ecoa-used-for)

### 8. [4K mediforms](https://www.g2.com/products/4k-mediforms/reviews)
4K mediforms is an Electronic Data Capture (EDC) system for clinical trials. The cloud-based system streamlines data collection with features like electronic case report forms, electronic patient reported outcomes, randomization tool, dashboards, user permissions, data exports, privacy controls, and audit trails. 4K mediforms follows EMA guidelines for validated computer systems used in regulated clinical studies. The software aims to make clinical trials more effective through certified electronic data collection.



**Who Is the Company Behind 4K mediforms?**

- **Seller:** [4K ANALYTICS GmbH](https://www.g2.com/sellers/4k-analytics-gmbh)
- **HQ Location:** Leipzig, DE
- **LinkedIn® Page:** https://de.linkedin.com/company/4k-analytics (44 employees on LinkedIn®)






### 9. [CapTrial](https://www.g2.com/products/captrial/reviews)
CapTrial is a cutting-edge software solution designed to revolutionize the way clinical data is managed. By leveraging the power of artificial intelligence and advanced data processing, CapTrial seamlessly extracts, organizes, and contextualizes data from electronic health records (EHRs), facilitating effortless retrieval of information, gaining valuable insights, and automating the generation of up-to-date electronic Case Report Forms (eCRFs) synchronized with EHR updates. CapTrial initiates at the data source, processing the connected EHR data extraction including patient anonymization. The data and metadata are securely encrypted and transmitted to the cloud, ensuring complete traceability and compliance. In the cloud, the data is processed and structured to automatically generate the eCRFs, reducing errors and alleviating the burdensome manual tasks associated with data entry and form generation. This enables researchers, medical professionals, and sponsors to concentrate on what truly matters: advancing healthcare innovation.



**Who Is the Company Behind CapTrial?**

- **Seller:** [Science4Tech](https://www.g2.com/sellers/science4tech)
- **Year Founded:** 2019
- **HQ Location:** Barcelona, ES
- **LinkedIn® Page:** https://www.linkedin.com/company/science4tech/ (32 employees on LinkedIn®)






### 10. [Catchtrial ePRO/eCOA](https://www.g2.com/products/catchtrial-epro-ecoa/reviews)
Catchtrial® ePRO/eCOA by Medigen Suite is a patient-friendly ePRO software platform for collecting electronic patient-reported outcomes and clinical outcome assessments in modern clinical trials. It delivers real-time symptom diaries, quality-of-life data, and validated instruments directly from patients on any device. Built for sponsors, CROs, biotech, pharmaceutical, and medical device organizations, the platform improves patient engagement, protocol compliance, and data quality. Catchtrial® ePRO/eCOA supports GDPR, HIPAA, ICH-GCP, and 21 CFR Part 11 requirements, helping teams capture reliable patient-reported outcomes across decentralized, hybrid, and site-based studies.



**Who Is the Company Behind Catchtrial ePRO/eCOA?**

- **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®)






### 11. [ClinAccess](https://www.g2.com/products/clinaccess/reviews)
Comprehensive SAS based clinical data management, EDC, and clinical trials reporting system



**Who Is the Company Behind ClinAccess?**

- **Seller:** [MAJARO InfoSystems](https://www.g2.com/sellers/majaro-infosystems)
- **HQ Location:** Santa Clara, US
- **LinkedIn® Page:** https://www.linkedin.com/company/145342 (1 employees on LinkedIn®)






### 12. [ClinicalHawk EDC](https://www.g2.com/products/clinicalhawk-edc/reviews)
Electronic Data Capture software streamlines the gathering of trial patient data for early to late-stage clinical research phases, as well as post-approval studies. An adaptable and scalable EDC system is used by Pharma, Biopharma, Medical Device Companies, across the clinical research industry.



**Who Is the Company Behind ClinicalHawk EDC?**

- **Seller:** [N2NAcers](https://www.g2.com/sellers/n2nacers)
- **Year Founded:** 2021
- **HQ Location:** Ahmedabad, IN
- **LinkedIn® Page:** https://www.linkedin.com/company/clinicalhawk (2 employees on LinkedIn®)






### 13. [Clinion ePRO](https://www.g2.com/products/clinion-clinion-epro/reviews)
Clinion ePRO is a secure platform designed to capture patient-reported outcomes directly from patients in real time. With support for mobile and web access, it enables seamless data collection while ensuring accuracy, compliance, and patient engagement across studies. What can you expect? ● Integrated or Standalone Deployment Use ePRO as a standalone solution or integrate seamlessly with Clinion EDC for unified data flow ● Direct Patient Data Capture Collect responses directly from patients through mobile or web, eliminating intermediaries and reducing data delays. ● BYOD Flexibility Allow patients to use their own devices, improving participation and reducing operational overhead. ● Real-Time Data Validation Validate responses instantly and sync data securely with Clinion EDC or operate in standalone mode. ● AI-Driven Data Checks Compare ePRO and EDC data to identify discrepancies early and reduce manual queries. ● Multilingual and Configurable Forms Deploy customized questionnaires with support for global studies and licensed instruments. Impact Improved patient compliance through reminders and an easy-to-use interface Reduced manual queries with early discrepancy detection Scalable across single-site and global trials



**Who Is the Company Behind Clinion ePRO?**

- **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®)






### 14. [Clinion eSource](https://www.g2.com/products/clinion-esource/reviews)
Clinion eSource enables site teams to capture clinical data directly at the point of care, reducing manual entry and delays. Built within a unified platform, it ensures accurate, complete, and audit-ready data from the start. What can you expect? ● Direct Data Capture at Source Enter data during patient visits to remove duplicate entry and reduce transcription errors. ● Real-Time Sync with EDC Sync source data directly with Clinion EDC to maintain consistency across systems. ● Faster Study Execution Reduce data cleaning effort and move studies forward with ready-to-use data. ● Reduced Monitoring Effort Enable focused monitoring with real-time visibility into site data. ● Audit-Ready Compliance Maintain full traceability with timestamps and version control aligned with regulations. ● Easy-to-Use Interface Simplify data entry with a clean interface designed for site users. Impact Reduced manual entry and transcription errors Faster database readiness Lower monitoring effort



**Who Is the Company Behind Clinion eSource?**

- **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®)






### 15. [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®)






### 16. [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 &amp; 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 \&gt; 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®)






### 17. [Cloudbyz EDC](https://www.g2.com/products/cloudbyz-edc/reviews)
Cloudbyz EDC is a cloud-native solution with an intuitive interface that is designed to store and manage clinical data effectively throughout a clinical trial’s life cycle. Our innovative solution enables clinical research teams to efficiently collect, analyze, and manage clinical data of different complexity and size. Build your study without code, with an interface that helps users build forms and easily navigate to the appropriate screens for data collection and analysis.



**Who Is the Company Behind Cloudbyz EDC?**

- **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®)






### 18. [Cronos](https://www.g2.com/products/webosphere-cronos/reviews)
Cronos is a clinical trial management software



**Who Is the Company Behind Cronos?**

- **Seller:** [Webosphere](https://www.g2.com/sellers/webosphere-7762f04b-f777-4daf-944d-ed8efec59588)
- **HQ Location:** Ahmedabad, IN
- **LinkedIn® Page:** http://www.linkedin.com/company/webosphere-inc- (80 employees on LinkedIn®)






### 19. [DADOS](https://www.g2.com/products/dados/reviews)
DADOS makes it easy for patients to fill out questionnaires directly on their tablet, from which clinicians and researchers can retrieve this information and build custom reports.



**Who Is the Company Behind DADOS?**

- **Seller:** [DADOS](https://www.g2.com/sellers/dados)
- **HQ Location:** Toronto, CA
- **LinkedIn® Page:** http://www.linkedin.com/company/dados-project (2 employees on LinkedIn®)






### 20. [Datacapt](https://www.g2.com/products/datacapt/reviews)
Join the New Clinical Trial Experience. Datacapt&amp;nbsp;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®)






### 21. [DATATRAK ONE Unified Experience](https://www.g2.com/products/datatrak-one-unified-experience/reviews)
DATATRAK provides industry-leading digital software for clinical trials. Responsive to the needs of each unique trial, we simplify the management of data for modern trials. Clients can make informed decisions faster with our standard and ad-hoc reporting capabilities, right through the interface, all with real-time data. We offer EDC, RTSM, a transformational CTMS solution, Trial Design, and Training, leveraging a single truth to eliminate redundant processes. See how DATATRAK can simplify the management of data for clinical trials.


**Average Rating:** 4.5/5.0
**Total Reviews:** 1
**How Do G2 Users Rate DATATRAK ONE Unified Experience?**

- **Quality of Support:** 10.0/10 (Category avg: 8.7/10)

**Who Is the Company Behind DATATRAK ONE Unified Experience?**

- **Seller:** [DATATRAK](https://www.g2.com/sellers/datatrak)
- **Year Founded:** 1991
- **HQ Location:** Cleveland , US
- **Twitter:** @DATATRAKinc (855 Twitter followers)
- **LinkedIn® Page:** https://www.linkedin.com/company/datatrak-international (280 employees on LinkedIn®)
- **Ownership:** OTC: DTRKD

**Who Uses This Product?**
- **Company Size:** 100% Small-Business



#### What Are Recent G2 Reviews of DATATRAK ONE Unified Experience?

**"[My experience with this program was Satisfactory.](https://www.g2.com/survey_responses/datatrak-one-unified-experience-review-157584)"**

**Rating:** 4.5/5.0 stars
*— Verified User in Health, Wellness and Fitness*

[Read full review](https://www.g2.com/survey_responses/datatrak-one-unified-experience-review-157584)

---


#### What Are G2 Users Discussing About DATATRAK ONE Unified Experience?

- [What is DATATRAK ONE Unified Experience used for?](https://www.g2.com/discussions/what-is-datatrak-one-unified-experience-used-for)

### 22. [DF mTrials AI](https://www.g2.com/products/df-mtrials-ai/reviews)
DF mTrials AI, EDC with Randomization and ePRO is a modern SaaS solution that can get you started on your clinical trial much faster than other tools in the market. The fully configurable product does not need a Clinical DB Programming team to setup the trial. Creating an eCRF is so easy that your trial team need not wait for weeks to enroll subjects and get started. DF mTrials AI brings forward a powerful set of tools to help customers harness data technology to turn research into reality.



**Who Is the Company Behind DF mTrials AI?**

- **Seller:** [Datafoundry](https://www.g2.com/sellers/datafoundry)
- **Year Founded:** 2016
- **HQ Location:** Bengaluru, IN
- **LinkedIn® Page:** https://www.linkedin.com/company/datafoundryai/?originalSubdomain=in (180 employees on LinkedIn®)






### 23. [Di-EDC](https://www.g2.com/products/di-edc/reviews)
Di-EDC is an Electronic Data Capture for clinical research made especially for researchers to manage Clinical Research Projects in a compliant environment. Increase your productivity using an intuitive interface with customizable forms, multiple projects support, access rights control, excel export/import, data validation ,full audit trail and more in just one system



**Who Is the Company Behind Di-EDC?**

- **Seller:** [DiData](https://www.g2.com/sellers/didata)
- **Year Founded:** 2019
- **HQ Location:** Lausanne, CH
- **LinkedIn® Page:** https://www.linkedin.com/company/swissdidata (23 employees on LinkedIn®)






### 24. [Digitalis](https://www.g2.com/products/digitalis/reviews)
Digitalis is an innovative data collection tool (Electronic Data Capture). Digitalis provides you with all the tools you need for a pleasant and complete collection and management of quality clinical data. It is a dynamic and ergonomic web application, whose strength lies in its ease of use and ability to adapt to your specific needs.



**Who Is the Company Behind Digitalis?**

- **Seller:** [Digitalis](https://www.g2.com/sellers/digitalis)
- **Year Founded:** 2017
- **HQ Location:** Limoges, FR
- **LinkedIn® Page:** http://www.linkedin.com/company/digitalis-clinical-data-collection (2 employees on LinkedIn®)






### 25. [Discovery for Clinical Studies](https://www.g2.com/products/discovery-for-clinical-studies/reviews)
RetinAI&#39;s Discovery for Clinical Studies is a comprehensive platform designed to streamline and enhance the management of clinical trials, particularly in ophthalmology. By centralizing data collection and analysis, it enables real-time decision-making and accelerates study timelines. The platform supports secure, global access for authorized users, eliminating the need for vendor-specific software and providing full control over data for additional analyses. Its integration of AI tools allows for simultaneous processing and automatic reading, potentially reducing costs associated with reading centers.



**Who Is the Company Behind Discovery for Clinical Studies?**

- **Seller:** [RetinAI](https://www.g2.com/sellers/retinai)
- **Year Founded:** 2017
- **HQ Location:** Bern, CH
- **LinkedIn® Page:** https://www.linkedin.com/company/11025877/ (48 employees on LinkedIn®)







## What Is Electronic Data Capture (EDC) Software?

[Clinical Research Software](https://www.g2.com/categories/clinical-research)

## What Software Categories Are Similar to Electronic Data Capture (EDC) Software?

- [Clinical Trial Management Systems](https://www.g2.com/categories/clinical-trial-management-systems)


---

## How Do You Choose the Right Electronic Data Capture (EDC) Software?

### What You Should Know About Electronic Data Capture (EDC) Software

### What is Electronic Data Capture (EDC) Software?

Electronic data capture (EDC) software collects and manages patient data for life sciences organizations during clinical trials, replacing traditional paper collection systems. This software improves data quality, streamlines data collection, and ensures regulatory compliance. Electronic data capture evolved from remote data entry (RDE) systems used in the 1980s, which allowed for local data collection on portable computers. EDC systems, by contrast, allow web forms to be created and accessed on the Internet, eliminating data silos and serving as a central hub for source data.

Depending on the EDC software, patient data may either be transcribed from paper forms or collected electronically at its source (e-source). This data is then saved as an electronic case report form (eCRF). Clinical trial participants may use connected devices to input responses, but study coordinators at research sites will commonly collect and manage data in the EDC system. Sponsors and contract research organizations (CROs) may also interact with the software for data verification, validation, or management.

EDC systems are most beneficial for assessing pharmaceutical and medical device safety, often in later phases of trials, but can be employed in various clinical trials. They significantly reduce the time needed for clinical study design and trial data collection while reducing human error and improving data workflows.&amp;nbsp;

### What are the Common Features of Electronic Data Capture (EDC) Software?

The following are some core features within EDC software that can help clinical trials manage data collection:

**eCRF builder:** eCRFs are intended to mimic paper forms, and EDC software provides point-and-click or drag-and-drop tools to build out case report forms and store templates for future use. Versioning allows eCRFs to be iteratively tested, with audit logs to track changes to forms over time. Collaboration tools allow multiple study and site staff to work from the same interface, building out forms exactly as they’ll appear to trial participants. eCRFs can be built to ensure erroneous data isn’t collected and specific triggers occur based on responses. Some EDC systems may also offer a library of standard form templates gathered from external sources.

**Data entry and collection:** Once eCRFs have been approved for use in clinical trials, data can be collected from trial participants and assigned to the right forms within the EDC system. Study coordinators can edit check data in real-time based on pre-designated protocols whenever discrepancies arise. Depending on the system, participant data can be collected from any device, with some allowing for randomization to protect clinical trial integrity. Modern EDC software also supports cloud data storage and API integration to support batch data importing and exporting.

**Data validation:** EDC software allows collected data to be checked against defined clinical trial protocols, ensuring both completeness and correctness of all captured clinical data. This ensures that trials are being conducted in compliance with regulatory requirements, most commonly 21 CFR Part 11. Data validation ensures no data is duplicated and that invalid data is not collected. This is often automatic within the system, preventing data that doesn’t meet all the defined parameters and formats from entering the database.

**Query management:** Given the complexity of clinical trials, multiple personas and stakeholders are involved in the process from start to finish. Query management features allow users in the EDC system to communicate with each other, raise and respond to questions, and address any issues with data before it is locked and finalized. Specific queries can be built into the system to trigger approval workflows, but manual queries can also be raised.

**Role-based permissions:** EDC software allows users to be assigned permissions based on their role, depending on if they are a site coordinator, data monitor, or another party. This promotes data security and integrity and reduces the likelihood of data tampering or breaches.

**Data reporting:** Data can be visualized and accessed in various formats, including dashboards, graphs, charts, and exported sheets. EDC software allows data to be imported or exported in several formats, and analytics helps measure ongoing trial outcomes. This data can be shared across different trial sites, and automatic updates can be configured in the system to send out triggers based on time or event.

### What are the Benefits of Electronic Data Capture (EDC) Software?

The following are the benefits of EDC software:

**Improved data quality:** Electronic data capture (EDC) software promotes data quality by eliminating outdated paper systems, which slow down trials. Duplicate and invalid data could take weeks to identify before electronic systems were introduced. An EDC system allows these issues to be raised and resolved in real time and even avoided entirely depending on how the parameters for valid responses to eCRFs are built.&amp;nbsp;

**Quicker data collection:** By consolidating data from multiple sources into one system, EDC software allows sites to complete trials quicker. Forms can be built and deployed faster, data entry is streamlined, querying and validation are resolved in real time, and data can be locked by the appropriate users—all within one system. Data can also be accessed much faster by searching within the database, allowing faster decisions to be made and for trials to be adapted as needed. EDC software unifies the various working parts that go into ideating and conducting clinical trials.&amp;nbsp;

**Improved data security and compliance:** EDC software promotes security standards that protect sensitive health data by offering audit trails, role-based permissions for data access, and built-in regulatory compliance standards (which may include 21 CFR part 11 compliance, GDPR compliance, and ISO 27001-2013 compliance). Data access is limited based on user type, and designated trial protocols ensure adherence to data integrity throughout the data collection process. Additionally, EDC vendors ensure data is protected and backed up, with more now offering cloud storage.

### Who Uses Electronic Data Capture (EDC) Software?

EDC software is used broadly across life sciences organizations, such as pharmaceutical, medtech, and biotechnology companies. There are three main personas involved in clinical trials and studies.

**Sites:** Sites coordinate the trial and are responsible for collecting data from clinical trial participants. These are typically hospitals or clinics, with nurses, physicians, and other designated site coordinators working to enter clinical data into the EDC system. Each trial site will have a principal investigator responsible for ensuring the site adheres to all trial protocols and reviews all collected data for approval.

**Sponsors:** A sponsor is an organization responsible for a clinical trial. This is typically the life sciences organization looking to have its medical product(s) approved for the market. Sponsors employ a number of staff who will work with an EDC system to monitor and manage data, conduct source data verification, and submit ongoing queries as needed to ensure data integrity.

**Contract research organizations (CROs):** CROs are essentially the middle-men between sites and sponsors. They are contracted by the sponsor organization to manage the clinical trial, often from planning to completion. CROs will often handle site visits on behalf of sponsors, in addition to a number of key trial management functions depending on the sponsor’s needs. CROs may use EDC software to support protocol development, clinical trial data management, data analysis, data querying, and ultimately monitor each trial site to ensure they remain compliant.

#### Software Related to Electronic Data Capture (EDC) Software

Related solutions that can be used together with electronic data capture software include:

[Clinical trial management software](https://www.g2.com/categories/clinical-trial-management) **:** Clinical trial management software (CTMS) works in tandem with EDC software to support the project management-related trial tasks. This can include participant screening and recruitment workflows, document management, financial management, and staff monitoring. EDC software should be able to interface with a clinical trial management system, promoting data exchange.

### Challenges with Electronic Data Capture (EDC) Software

Software solutions can come with their own set of challenges.&amp;nbsp;

**Initial implementation and adoption:** Utilizing EDC software requires every site to be trained on how to use it at each role level. This can be an ongoing process repeated each time a new trial is conducted.&amp;nbsp;

**International compliance:** If trial sites exist inside and outside the US, an EDC system may not provide all the necessary compliance support. For in-house designed EDCs, this is even more likely.&amp;nbsp;

**Browser compatibility:** Since EDC software is web based, browser compatibility and security are essential. A stable internet connection and uninterrupted access to a particular browser are needed, as well as data privacy standards depending on the browser.

### Which Companies Should Buy Electronic Data Capture (EDC) Software?

While EDC software users fall under the three personas of sites, sponsors, and CROs, the companies prompting the trials fall under the broader life sciences umbrella.

**Pharmaceutical companies:** Pharmaceutical companies involved in clinical trials use EDC software to collect data around drug testing. This is important in later phases of trials where pharmacovigilance matters.

**Medtech companies:** Medtech companies collect trial data with EDC software to ensure medical devices operate as intended and provide the advertised benefits. This extends beyond clinical trials and into post-market safety surveillance as well, once devices have been made available to the general public.

**Biotech companies:** Biotech companies that don’t fall under pharmaceutical or medical device development may also use EDC software in their clinical research trials. Vaccine testing is one important example where multiple trial phase data collection is important for getting vaccines approved. Biotech companies conducting other R&amp;D trials rely on EDC software to ensure ethical testing.

### How to Buy Electronic Data Capture (EDC) Software

#### Requirements Gathering (RFI/RFP) for Electronic Data Capture (EDC) Software

Whether a company is just starting to explore electronic data capture (EDC) software or is looking for a more appropriate solution for their needs, G2.com can help inform buyers of the market and assist them in selecting the best software product for their business.

For EDC software, the core functionality does not differ much across products. They promote data capture and validation and will likely only differ in areas such as cloud storage, device compatibility and integrations, and advanced user permissions. Buyers should consider what is working and not working with their current EDC system and use that as a starting point. Some of the questions to explore could be—does the organization need a different EDC to integrate with its existing clinical trial management tools? Does the current system lack key data management features? Is the current system too complex for certain users?

#### Compare Electronic Data Capture (EDC) Software Products

**Create a long list**

The first step to finding the perfect software solution is to create a preliminary list of products that fit the buyer’s general needs. The next step is to narrow down the list by selecting specific features that are must-haves or requirements for the buyer. G2.com provides information about the best electronic data capture (EDC) software, allowing buyers to filter options and user reviews to help narrow the product list to a more relevant selection.

**Create a short list**

Creating a short list of software products is an important step in the buying process. While it may be daunting to filter through various products, users can get help by utilizing G2’s compare feature. This feature will take products of choice and display them side by side so the buyer can easily determine which software ticks the important boxes on the list.

**Conduct demos**

Once the buyer has narrowed down the product list, the next step is to conduct a demo. Demos allow buyers to see a product and its features in more detail. To ensure a buyer gets the most out of a demo, it’s important to go in prepared. Buyers should be prepared to thoroughly test each product from the perspective of multiple trial users. Some of the questions to keep in mind would be how intuitive is the system for site staff as opposed to sponsor or CRO staff? How elaborate are the eCRF design features? Additionally, buyers should inquire about cost, integrations, vendor support, and any concerns they have about the product. Adequate preparation will make it easier for a buyer to compare products after completing the demos.

#### Selection of Electronic Data Capture (EDC) Software

**Choose a selection team**

A combination of sponsor and CRO staff will most likely be involved in selecting the appropriate EDC software for trial use, as they have the biggest stake in ensuring trials are completed satisfactorily. This will include higher-tier roles involved in data management and validation but may also ultimately fall upon the CRO’s recommendation if the sponsor defers to their expertise.&amp;nbsp;

**Negotiation**

Once the selection team has narrowed down their software picks, it’s time to discuss customization options, pricing, and the type of support needed from the vendor. It’s always important to address pricing options, even when they are listed on a vendor’s website. Many software vendors will provide discounts and custom pricing options based on what the buyer is looking to purchase.

**Final decision**

Once a buyer has made the final decision on a product and is ready to move forward with a purchase, it is recommended to conduct a final demo, enquire about a trial run, and determine the next steps if the product doesn’t ultimately fit their needs. These steps can give a buyer an additional sense of security and confidence when making a final decision.




