# Best Electronic Data Capture (EDC) Software

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

**Total Products under this Category:** 119

### Category Stats (Aug 2026)

- **Average Rating:** 4.29/5 (↑0.01 vs Jul 2026) The average rating of products in this category, based on all submitted ratings
- **Top Trending Product:** cubeCDMS (+1.03%) - Among all products in this category, cubeCDMS recorded the largest rating increase compared to last month

_Last updated: August 01, 2026_

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

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

- 30 Analysts and Data Experts
- 1,800+ Authentic Reviews
- 119+ 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 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=51250&focus%5B%5D=1366872&focus%5B%5D=94249&focus%5B%5D=44344&focus%5B%5D=90824&focus%5B%5D=128837&focus%5B%5D=26533&focus%5B%5D=43817)

Highlighted products: Medrio EDC, cubeCDMS, Viedoc, Greenlight Guru Clinical, Medidata Rave, Oracle Clinical, Castor, and iMednet EDC.

Underlying data: [Grid® JSON](https://www.g2.com/categories/electronic-data-capture-edc/grids.json?focus%5B%5D=medrio-edc&focus%5B%5D=cubecdms&focus%5B%5D=viedoc&focus%5B%5D=greenlight-guru-clinical&focus%5B%5D=medidata-rave&focus%5B%5D=oracle-clinical&focus%5B%5D=castor-edc-castor&focus%5B%5D=imednet-edc)

**Sponsored**

### REDCap Cloud EDC

REDCap Cloud offers a unified clinical research platform that brings together EDC, Randomization, ePRO and eConsent into a continuous data ecosystem, enabling real-time intelligence across the full lifecycle of IIT/IIS, RCT and RWE studies. Designed to support global Clinical Research for MedTech, Academic / IIS/ IIT, Biotech, Health Systems, Registries and RWE projects.

[Visit website](https://www.g2.com/external_clickthroughs/record?secure%5Bad_program%5D=ppc&secure%5Bad_slot%5D=category_product_list_llm&secure%5Bcategory_id%5D=1733&secure%5Bchosen_at%5D=2026-08-01T23%3A56%3A43Z&secure%5Bdisplayable_resource_id%5D=1733&secure%5Bdisplayable_resource_type%5D=Category&secure%5Bmedium%5D=sponsored&secure%5Bplacement_reason%5D=page_category&secure%5Bplacement_resource_ids%5D%5B%5D=1733&secure%5Bprioritized%5D=false&secure%5Bproduct_id%5D=1870742&secure%5Bresource_id%5D=1733&secure%5Bresource_type%5D=Category&secure%5Bsource_type%5D=category_page&secure%5Bsource_url%5D=https%3A%2F%2Fwww.g2.com%2Fcategories%2Felectronic-data-capture-edc%3Fopen_modal_url%3D%252Fproducts%252Fvelos-eresearch%252Fwishlists%253Fhost_path%253D%25252Fcategories%25252Felectronic-data-capture-edc%2526source%253Dcategory&secure%5Btoken%5D=0475b721ff43298ef432481fb403b022bff6ebaeebfb2ee17c65ee56721ca522&secure%5Burl%5D=https%3A%2F%2Fwww.redcapcloud.com%2F%3Futm_source%3Dg2%26utm_medium%3Dpaid%26utm_campaign%3Dg2-sponsored-edcm%26utm_content%3Dcategory-listing&secure%5Burl_type%5D=custom_url)

### [Medrio EDC](https://www.g2.com/es/products/medrio-edc/reviews)

Más que solo un sistema EDC, Medrio EDC es un sistema completo de gestión de datos clínicos diseñado para equipos pequeños y en crecimiento. Está conectado a una plataforma intuitiva y sin código que te da control total desde la construcción de la base de datos hasta tu informe final. Una plataforma que incluye ePRO, eConsent, RTSM, CTSM y eTMF. Realiza todos tus estudios con confianza con un EDC completamente validado y listo para auditorías, respaldado por más de 20 años de uso clínico en miles de ensayos clínicos completados. Ofrecemos soporte experto y salidas de datos de alta calidad sin costos ocultos, complejidad añadida o riesgo. Los principales innovadores de la industria utilizan Medrio EDC, incluidos aquellos dentro de los sectores farmacéutico, biotecnológico, medtech, dispositivos médicos, diagnósticos, salud animal y todos los principales sectores de ciencias de la vida. Nos comprometemos activamente con nuestros clientes, escuchamos sus comentarios e incorporamos sus necesidades en nuestras soluciones. Lanza en horas o días, no semanas o meses. Puedes completar la construcción de estudios en menos de 3 semanas, en comparación con el promedio de la industria de 12, con nuestra base sin código y funcionalidad de copia de estudio. Los flujos de trabajo automatizados eliminan ineficiencias sin comprometer nunca la calidad de los datos. Realiza cambios en medio del estudio en tan solo un día, con un tiempo de inactividad mínimo. Mantente informado en cada etapa. Los paneles basados en permisos, las exportaciones con un solo clic y la visibilidad de datos casi en tiempo real mantienen a todo tu equipo alineado y avanzando. La base tecnológica adecuada hace que todo sea posible, incluidos los plazos más cortos que te permiten escalar tus ensayos con facilidad. No importa el tamaño o la fase del estudio, Medrio protege tus datos en cada paso del camino.

**Average Rating:** 4.2/5.0

**Total Reviews:** 254

#### How Do G2 Users Rate Medrio EDC?

- **Captura de datos - Captura electrónica de datos (EDC):** 8.8/10 (Category avg: 8.9/10)
- **Cumplimiento - Captura electrónica de datos (EDC):** 9.0/10 (Category avg: 8.7/10)
- **eCRFs - Captura Electrónica de Datos (EDC):** 8.7/10 (Category avg: 8.8/10)
- **Calidad del soporte:** 8.9/10 (Category avg: 8.6/10)

#### Who Is the Company Behind Medrio EDC?

- **Vendedor:** [Medrio](https://www.g2.com/es/sellers/medrio)
- **Sitio web de la empresa:** medrio.com
- **Año de fundación:** 2005
- **Ubicación de la sede:** San Francisco, CA
- **Twitter:** @medrio  
1,011 seguidores en Twitter
- **Página de LinkedIn®:** [www.linkedin.com](https://www.g2.com/es/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=337c2e01498f8d77b321cab95701e78d2a1ef19efb754a25bf2f18da8e4815db&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F132347%2F&secure%5Burl_type%5D=linkedin_company_website)  
182 empleados en LinkedIn®

#### Who Uses This Product?

- **Who Uses This:** Gerente de Datos Clínicos
- **Top Industries:** Investigación, Biotecnología
- **Company Size:** 40% Small, 30% Medium

#### What Do G2 Reviewers Say About Medrio EDC?

_AI-generated summary from verified user reviews_

##### Pros

- Los usuarios aprecian la **facilidad de uso** de Medrio EDC, destacando su interfaz intuitiva y funcionalidad confiable.
- Los usuarios elogian el **servicio de atención al cliente fácil de usar** de Medrio EDC, destacando respuestas rápidas y un servicio útil.
- Los usuarios aprecian la **interfaz de usuario intuitiva** de Medrio EDC, lo que la hace fácil y confiable para los recién llegados.
- Los usuarios aprecian la **facilidad de construcción** en Medrio EDC, encontrando el proceso intuitivo y altamente flexible.
- Los usuarios valoran la **gestión eficiente de datos** y el diseño fácil de usar de Medrio EDC para una configuración de estudio sin problemas.

##### Cons

- Los usuarios encuentran la **funcionalidad de informes inadecuada** , lo que lleva a depender de los filtros para una gestión de datos efectiva.
- Los usuarios encuentran las **herramientas de navegación e informes difíciles** de usar en Medrio EDC, particularmente en iPads.
- Los usuarios notan las **características faltantes** en Medrio EDC, deseando una interfaz mejorada y mejores opciones de integración.
- Los usuarios encuentran que las **limitaciones para estudios complejos o grandes** obstaculizan la funcionalidad general de Medrio EDC.
- Los usuarios enfrentan **problemas de gestión de datos** con Medrio EDC, incluyendo ineficiencias en el manejo de estudios complejos y la carga de informes.

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

**["La interfaz simple facilita la creación de formularios y la configuración de estudios."](https://www.g2.com/es/survey_responses/medrio-edc-review-13136203)**

**Rating:** 4.0/5.0 stars

_— Usuario verificado en Dispositivos médicos_

[Read full review](https://www.g2.com/es/survey_responses/medrio-edc-review-13136203)

**["Portal fácil de navegar, se necesitan mejoras menores (seguimiento)"](https://www.g2.com/es/survey_responses/medrio-edc-review-12370852)**

**Rating:** 4.0/5.0 stars

_— Usuario verificado en Biotecnología_

[Read full review](https://www.g2.com/es/survey_responses/medrio-edc-review-12370852)

#### What Are G2 Users Discussing About Medrio EDC?

- [What is the difference between CTMS and EDC?](https://www.g2.com/es/discussions/medrio-edc-what-is-the-difference-between-ctms-and-edc)
- [What does an EDC system do?](https://www.g2.com/es/discussions/what-does-an-edc-system-do)
- [What is EDC Medrio?](https://www.g2.com/es/discussions/what-is-edc-medrio)

### [cubeCDMS](https://www.g2.com/es/products/cubecdms/reviews)

cubeCDMS es ampliamente reconocido por los gestores de datos clínicos e investigadores como un fuerte candidato para el mejor sistema EDC (Captura Electrónica de Datos) para ensayos clínicos modernos. Al combinar sin problemas la tecnología de IA de vanguardia con una interfaz intuitiva y centrada en el usuario, empoderamos a los equipos de operaciones clínicas para acelerar los avances médicos. Confiado en más de 6,000 ensayos clínicos por una base de clientes global en rápido crecimiento, cubeCDMS es el EDC preferido por los usuarios para ofrecer una configuración rápida, calidad de datos impecable y escalabilidad económica. Por qué los equipos de investigación de élite eligen cubeCDMS: - Configuración EDC y Garantía de Calidad lideradas por IA: CRScube está a la vanguardia de la integración de IA en la investigación clínica. cubeCDMS cuenta con una configuración EDC liderada por IA propia que reduce drásticamente el tiempo de configuración del sistema y aumenta fundamentalmente la calidad de los datos y la construcción desde el primer día. Al automatizar la configuración básica, eliminamos los cuellos de botella manuales tradicionales y el error humano. - Automatización Inteligente de Datos: Más allá de la configuración, nuestra plataforma aprovecha la codificación médica impulsada por IA y la automatización inteligente para agilizar la gestión de datos. Este enfoque continuo en IA minimiza los volúmenes de consultas, acelera la limpieza de datos y asegura una estricta adherencia a los estándares del protocolo. - Satisfacción Excepcional del Usuario: Respaldado por elogios consistentemente altos de usuarios verificados en G2, cubeCDMS es celebrado por su facilidad de uso y soporte estelar. Los clientes frecuentemente destacan nuestro equipo de atención al cliente altamente receptivo y nuestro enfoque proactivo para implementar comentarios de los usuarios, asegurando una experiencia fluida tanto para los gestores de estudio como para el personal del sitio. - Flexibilidad Sin Código: Despliega tus estudios con la máxima agilidad. cubeCDMS ofrece un entorno completamente sin código que cuenta con una biblioteca de eCRF pre-validada, permitiendo a los equipos adaptarse rápidamente a enmiendas de protocolo y diseños de estudio complejos sin requerir habilidades avanzadas de programación. - Flujo de Trabajo Clínico Unificado: Optimiza tus ensayos con una suite integral que incluye detección automática de violaciones de protocolo, gestión de consultas por lotes, monitoreo basado en riesgos (RBM) nativo e integración perfecta en una sola plataforma con otros productos de CRScube. Ya sea que busques reducir costos operativos, mejorar la colaboración en el sitio o preparar tus ensayos para el futuro con inteligencia artificial, cubeCDMS ofrece una plataforma centralizada y altamente configurable diseñada para el futuro de la investigación clínica. ¡Visita nuestro sitio web para ver por qué somos una solución EDC de alta calificación!

**Average Rating:** 4.7/5.0

**Total Reviews:** 184

#### How Do G2 Users Rate cubeCDMS?

- **Captura de datos - Captura electrónica de datos (EDC):** 9.3/10 (Category avg: 8.9/10)
- **Cumplimiento - Captura electrónica de datos (EDC):** 9.2/10 (Category avg: 8.7/10)
- **eCRFs - Captura Electrónica de Datos (EDC):** 9.4/10 (Category avg: 8.8/10)
- **Calidad del soporte:** 9.3/10 (Category avg: 8.6/10)

#### Who Is the Company Behind cubeCDMS?

- **Vendedor:** [CRScube](https://www.g2.com/es/sellers/crscube)
- **Sitio web de la empresa:** www.crscube.io
- **Año de fundación:** 2010
- **Ubicación de la sede:** Seoul, KR
- **Página de LinkedIn®:** [www.linkedin.com](https://www.g2.com/es/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=3f35166d622fd9d16a5de659f76d5f44c02b29b6b15ac17563bc1ecfce91dd28&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fcrscube%2F&secure%5Burl_type%5D=linkedin_company_website)  
85 empleados en LinkedIn®

#### Who Uses This Product?

- **Who Uses This:** CRA, CRC
- **Top Industries:** Farmacéuticos, Biotecnología
- **Company Size:** 49% Medium, 44% Small

#### What Do G2 Reviewers Say About cubeCDMS?

_AI-generated summary from verified user reviews_

##### Pros

- Los usuarios aprecian la **facilidad de uso** de cubeCDMS, disfrutando de su interfaz intuitiva y gestión eficiente de estudios.
- Los usuarios aprecian la **interfaz intuitiva** de cubeCDMS, que permite una gestión eficiente de estudios y una experiencia de usuario sin problemas.
- Los usuarios aprecian la **interfaz de usuario intuitiva y sencilla** de cubeCDMS, mejorando la navegación y la gestión de tareas.
- Los usuarios valoran el **fácil acceso visual a los datos** y el monitoreo en tiempo real integrado de cubeCDMS para un seguimiento eficiente.
- Los usuarios valoran el **soporte al cliente rápido y claro** de CubeCDMS, mejorando su experiencia general con el sistema.

##### Cons

- Los usuarios encuentran el **sistema de reseñas complicado** y el manual difícil de leer, lo que afecta la usabilidad.
- Los usuarios sienten que las **funciones faltantes** en cubeCDMS limitan la funcionalidad, sugiriendo mejoras para una mayor conveniencia.
- Los usuarios están frustrados por las **limitaciones de consulta** que dificultan la visibilidad y el seguimiento de las respuestas después de que se completan las consultas.
- Los usuarios están frustrados con el **rendimiento lento** de cubeCDMS, particularmente durante las descargas de conjuntos de datos y las respuestas del sistema.
- Los usuarios expresan preocupaciones sobre **problemas de gestión de datos** , señalando el riesgo de respuestas comprometidas a consultas y la emisión engorrosa de informes.

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

**["Un CDMS bien diseñado que realmente mejora la experiencia del usuario y el flujo de trabajo diario"](https://www.g2.com/es/survey_responses/cubecdms-review-13067242)**

**Rating:** 5.0/5.0 stars

_— 송희 ._

[Read full review](https://www.g2.com/es/survey_responses/cubecdms-review-13067242)

**["Integración y utilización conveniente de varios sistemas"](https://www.g2.com/es/survey_responses/cubecdms-review-13128600)**

**Rating:** 5.0/5.0 stars

_— suji K._

[Read full review](https://www.g2.com/es/survey_responses/cubecdms-review-13128600)

### [Viedoc](https://www.g2.com/es/products/viedoc/reviews)

Viedoc diseña software atractivo para la industria de las ciencias de la vida. Al acelerar los ensayos clínicos en todos los niveles, las soluciones de Viedoc apoyan a importantes empresas farmacéuticas, biotecnológicas y de dispositivos médicos, así como a reconocidas instituciones de investigación en todo el mundo. Desde la creación de Viedoc en 2003, más de 1 millón de pacientes en más de 75 países han participado en estudios impulsados por Viedoc.

**Average Rating:** 4.5/5.0

**Total Reviews:** 225

#### How Do G2 Users Rate Viedoc?

- **Captura de datos - Captura electrónica de datos (EDC):** 9.2/10 (Category avg: 8.9/10)
- **Cumplimiento - Captura electrónica de datos (EDC):** 9.1/10 (Category avg: 8.7/10)
- **eCRFs - Captura Electrónica de Datos (EDC):** 9.1/10 (Category avg: 8.8/10)
- **Calidad del soporte:** 9.2/10 (Category avg: 8.6/10)

#### Who Is the Company Behind Viedoc?

- **Vendedor:** [Viedoc Technologies](https://www.g2.com/es/sellers/viedoc-technologies)
- **Sitio web de la empresa:** www.viedoc.com
- **Año de fundación:** 2003
- **Ubicación de la sede:** Uppsala, Uppsala County
- **Twitter:** @ViedocOfficial  
200 seguidores en Twitter
- **Página de LinkedIn®:** [www.linkedin.com](https://www.g2.com/es/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=c371e8b975f866a496be8f70bcf37fb6d041738a72a0ce228cd4700d91f55e63&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fviedoctechnologies%2F&secure%5Burl_type%5D=linkedin_company_website)  
129 empleados en LinkedIn®

#### Who Uses This Product?

- **Who Uses This:** Gerente de Datos, Analista Asociado
- **Top Industries:** Farmacéuticos, Investigación
- **Company Size:** 37% Large, 33% Medium

#### What Do G2 Reviewers Say About Viedoc?

_AI-generated summary from verified user reviews_

##### Pros

- Los usuarios aprecian la **facilidad de uso** en Viedoc, lo que permite una configuración rápida y la automatización de tareas repetitivas.
- Los usuarios aprecian la **interfaz fácil de usar** de Viedoc, destacando su diseño intuitivo y fácil navegación.
- Los usuarios valoran el **diseño intuitivo** de Viedoc, lo que permite una configuración rápida y una navegación eficiente para estructuras de estudio complejas.
- El **soporte al cliente** de Viedoc es excepcional, ofreciendo asistencia receptiva y recursos valiosos para una experiencia de usuario fluida.
- Los usuarios valoran el **diseño fácil de usar** de Viedoc, que simplifica la gestión de datos clínicos y mejora la eficiencia general del flujo de trabajo.

##### Cons

- Los usuarios experimentan **rendimiento lento** con Viedoc, particularmente al procesar grandes conjuntos de datos o al abrir nuevas ventanas.
- Los usuarios encuentran **difíciles de navegar las configuraciones** y reportan un rendimiento lento con los modelos de informes.
- Los usuarios sienten que el **control de acceso basado en roles** en Viedoc puede ser limitante, afectando la colaboración y la eficiencia del flujo de trabajo.
- Los usuarios encuentran que los **problemas de diseño de formularios** de Viedoc son restrictivos y experimentan desafíos con la interfaz de usuario desactualizada y la gestión de errores.
- Los usuarios enfrentan **características faltantes** en Viedoc, lo que complica la creación de formularios y la integración con otras plataformas.

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

**["Diseño simple y versátil y un producto que se mantiene al día con un mercado en rápido movimiento"](https://www.g2.com/es/survey_responses/viedoc-review-12611501)**

**Rating:** 4.5/5.0 stars

_— Marina A._

[Read full review](https://www.g2.com/es/survey_responses/viedoc-review-12611501)

**["Impulsar la Eficiencia y la Calidad de los Datos en la Gestión de Ensayos Clínicos"](https://www.g2.com/es/survey_responses/viedoc-review-8698783)**

**Rating:** 5.0/5.0 stars

_— DEEKSHITHA V._

[Read full review](https://www.g2.com/es/survey_responses/viedoc-review-8698783)

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

- [¿Para qué se utiliza Viedoc?](https://www.g2.com/es/discussions/what-is-viedoc-used-for) - 1 comment

### [Greenlight Guru Clinical](https://www.g2.com/products/greenlight-guru-clinical/reviews)

The only Electronic Data Capture (EDC) system designed specifically for Medical Devices & Diagnostics. A complete electronic data collection toolbox for Post-Market Clinical Follow-Up (PMCF), Post-Market Performance Follow-Up (PMPF), Clinical Investigations and Clinical Performance Studies.

**Average Rating:** 4.3/5.0

**Total Reviews:** 116

#### How Do G2 Users Rate Greenlight Guru Clinical?

- **Data Capture - Electronic Data Capture (EDC):** 8.6/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 8.5/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 8.6/10 (Category avg: 8.8/10)
- **Quality of Support:** 9.3/10 (Category avg: 8.6/10)

#### Who Is the Company Behind Greenlight Guru Clinical?

- **Seller:** [Greenlight Guru](https://www.g2.com/sellers/greenlight-guru)
- **Company Website:** www.greenlight.guru
- **Year Founded:** 2013
- **HQ Location:** Indianapolis, IN
- **Twitter:** @greenlightguru  
10,590 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=7df50f335a6d5a650bbc46a24d2ab5da06b02fc852b348529906f73428faacd5&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F3837459%2F&secure%5Burl_type%5D=linkedin_company_website)  
139 employees on LinkedIn®

#### Who Uses This Product?

- **Top Industries:** Medical Devices, Research
- **Company Size:** 64% Small, 24% Medium

#### What Do G2 Reviewers Say About Greenlight Guru Clinical?

_AI-generated summary from verified user reviews_

##### Pros

- Users find the **ease of implementation** with Greenlight Guru Clinical to be straightforward and user-friendly.

##### Cons

- Users criticize the **awful navigation** in Greenlight Guru Clinical, making subject reviews cumbersome and inefficient.
- Users find **missing features** in Greenlight Guru Clinical, such as poor navigation and lack of review options, frustrating.
- Users find **navigation confusing** , requiring multiple steps that hinder data review efficiency and overall user experience.

#### What Are Recent G2 Reviews of Greenlight Guru Clinical?

**["Site Data Entry User Experience"](https://www.g2.com/survey_responses/greenlight-guru-clinical-review-12624398)**

**Rating:** 4.5/5.0 stars

_— Darwin M._

[Read full review](https://www.g2.com/survey_responses/greenlight-guru-clinical-review-12624398)

**["Greenlight Guru survey"](https://www.g2.com/survey_responses/greenlight-guru-clinical-review-8876669)**

**Rating:** 5.0/5.0 stars

_— rabab h._

[Read full review](https://www.g2.com/survey_responses/greenlight-guru-clinical-review-8876669)

### [Medidata Rave](https://www.g2.com/es/products/medidata-rave/reviews)

Medidata Rave es un sistema de gestión de datos clínicos basado en la nube que se utiliza para capturar, gestionar e informar datos de investigación clínica de manera electrónica. Permite al usuario registrar información del paciente (es decir, datos de visitas, laboratorios y eventos adversos) utilizando formularios que se personalizan para cada estudio.

**Average Rating:** 4.7/5.0

**Total Reviews:** 25

#### How Do G2 Users Rate Medidata Rave?

- **Captura de datos - Captura electrónica de datos (EDC):** 9.1/10 (Category avg: 8.9/10)
- **Cumplimiento - Captura electrónica de datos (EDC):** 9.0/10 (Category avg: 8.7/10)
- **eCRFs - Captura Electrónica de Datos (EDC):** 9.3/10 (Category avg: 8.8/10)
- **Calidad del soporte:** 9.0/10 (Category avg: 8.6/10)

#### Who Is the Company Behind Medidata Rave?

- **Vendedor:** [Medidata](https://www.g2.com/es/sellers/medidata)
- **Año de fundación:** 1999
- **Ubicación de la sede:** New York, NY
- **Twitter:** @Medidata  
11,517 seguidores en Twitter
- **Página de LinkedIn®:** [www.linkedin.com](https://www.g2.com/es/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=97df152039f63dd4263d30a4bcff376de85ffbb6cf576a90b313a4fe6fc84d8f&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F12076%2F&secure%5Burl_type%5D=linkedin_company_website)  
2,803 empleados en LinkedIn®

#### Who Uses This Product?

- **Top Industries:** Atención hospitalaria y sanitaria, Farmacéuticos
- **Company Size:** 52% Large, 26% Medium

#### What Do G2 Reviewers Say About Medidata Rave?

_AI-generated summary from verified user reviews_

##### Pros

- Los usuarios valoran las capacidades de **gestión de datos integrados** de Medidata Rave para un análisis integral de ensayos clínicos.
- Los usuarios valoran las **fáciles integraciones** de Medidata Rave, mejorando el análisis de datos clínicos en diversos tamaños de estudio.

##### Cons

- Los usuarios destacan los **altos costos** de Medidata Rave, lo que hace que sea un desafío para las pequeñas empresas poder costearlo.
- Los usuarios enfrentan **problemas de inicio de sesión** con cierres de sesión rápidos debido a la inactividad, lo que afecta su flujo de trabajo y accesibilidad.

#### What Are Recent G2 Reviews of Medidata Rave?

**["Mi experiencia en Rave"](https://www.g2.com/es/survey_responses/medidata-rave-review-8672835)**

**Rating:** 5.0/5.0 stars

_— Usuario verificado en Biotecnología_

[Read full review](https://www.g2.com/es/survey_responses/medidata-rave-review-8672835)

**["Fácil de navegar y aprender—Sin quejas sobre Medidata"](https://www.g2.com/es/survey_responses/medidata-rave-review-12510795)**

**Rating:** 5.0/5.0 stars

_— sydney n._

[Read full review](https://www.g2.com/es/survey_responses/medidata-rave-review-12510795)

#### What Are G2 Users Discussing About Medidata Rave?

- [Is Medidata Rave a CTMS?](https://www.g2.com/es/discussions/medidata-rave-is-medidata-rave-a-ctms)
- [Is Medidata Rave a CTMS?](https://www.g2.com/es/discussions/is-medidata-rave-a-ctms)
- [What is the difference between CTMS and EDC?](https://www.g2.com/es/discussions/what-is-the-difference-between-ctms-and-edc)
- [What is Medidata Rave EDC?](https://www.g2.com/es/discussions/what-is-medidata-rave-edc)
- [¿Qué es rave en CDM?](https://www.g2.com/es/discussions/what-is-rave-in-cdm) - 1 comment

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

Oracle Remote Data Capture provides a single application and infrastructure for electronic data capture and clinical data management.

**Average Rating:** 4.1/5.0

**Total Reviews:** 23

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

- **Data Capture - Electronic Data Capture (EDC):** 8.3/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 8.7/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 8.9/10 (Category avg: 8.8/10)
- **Quality of Support:** 8.2/10 (Category avg: 8.6/10)

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

- **Seller:** [Oracle](https://www.g2.com/sellers/oracle)
- **Year Founded:** 1977
- **HQ Location:** Austin, TX
- **Twitter:** @Oracle  
827,997 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=a14fcbcd818b49d781453c19628a9479a70cc1e8e335e54c876392ab5f543da3&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F1028%2F&secure%5Burl_type%5D=linkedin_company_website)  
208,078 employees on LinkedIn®
- **Ownership:** NYSE:ORCL

#### Who Uses This Product?

- **Top Industries:** Pharmaceuticals, Hospital & Health Care
- **Company Size:** 41% Large, 38% Medium

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

**["Its excellent. I am working with Oracle Clinical platforms more than 5 years."](https://www.g2.com/survey_responses/oracle-clinical-review-4426626)**

**Rating:** 5.0/5.0 stars

_— Rajdip C._

[Read full review](https://www.g2.com/survey_responses/oracle-clinical-review-4426626)

**["Oracle clinical review"](https://www.g2.com/survey_responses/oracle-clinical-review-4413512)**

**Rating:** 4.0/5.0 stars

_— Verified User in Pharmaceuticals_

[Read full review](https://www.g2.com/survey_responses/oracle-clinical-review-4413512)

#### What Are G2 Users Discussing About Oracle Clinical?

- [What is Oracle Data Management Workbench?](https://www.g2.com/discussions/what-is-oracle-data-management-workbench)
- [What is Oracle Clinical one?](https://www.g2.com/discussions/what-is-oracle-clinical-one)
- [What is Oracle Clinical RDC?](https://www.g2.com/discussions/what-is-oracle-clinical-rdc)

### [Castor](https://www.g2.com/es/products/castor-edc-castor/reviews)

Castor es una plataforma líder de datos clínicos basada en la nube, diseñada para democratizar la investigación y simplificar las complejidades de los ensayos clínicos descentralizados, híbridos y tradicionales. Confiada por instituciones académicas, empresas biotecnológicas y farmacéuticas de todo el mundo, Castor permite a los investigadores capturar datos de alta calidad y acelerar los tiempos de estudio a través de un ecosistema modular y centrado en el ser humano. Nuestra plataforma plug-and-play integra sin problemas los cuatro componentes críticos de la investigación clínica moderna: Captura Electrónica de Datos (EDC): Un sistema EDC de despliegue rápido y fácil de usar que permite a los investigadores construir y lanzar estudios en cuestión de clics, no meses, asegurando una sólida integridad y seguridad de los datos. eConsentimiento: Una solución flexible de consentimiento electrónico que simplifica la inscripción de pacientes y mejora la comprensión, apoyando estrategias de reclutamiento remoto y en el sitio para maximizar la participación. eCOA (Evaluación Electrónica de Resultados Clínicos): Herramientas intuitivas para capturar Resultados Informados por los Pacientes (PROs) directamente de los participantes, mejorando el compromiso y la retención mientras se reduce la carga de entrada de datos. Evidencia del Mundo Real (RWE): Capacidades avanzadas para capturar y unificar datos del mundo real de dispositivos portátiles, dispositivos médicos e historias clínicas electrónicas (EHRs), proporcionando una visión holística de la salud del paciente más allá del entorno clínico. Al priorizar un enfoque "primero el participante", Castor mejora la experiencia del ensayo tanto para los investigadores como para los pacientes. Desde la rápida construcción y inscripción del estudio hasta el análisis final, Castor ofrece la velocidad, escalabilidad y cumplimiento necesarios para impulsar resultados exitosos en el cambiante panorama de la investigación clínica.

**Average Rating:** 4.6/5.0

**Total Reviews:** 125

#### How Do G2 Users Rate Castor?

- **Captura de datos - Captura electrónica de datos (EDC):** 9.4/10 (Category avg: 8.9/10)
- **Cumplimiento - Captura electrónica de datos (EDC):** 9.1/10 (Category avg: 8.7/10)
- **eCRFs - Captura Electrónica de Datos (EDC):** 9.2/10 (Category avg: 8.8/10)
- **Calidad del soporte:** 9.2/10 (Category avg: 8.6/10)

#### Who Is the Company Behind Castor?

- **Vendedor:** [Castor EDC](https://www.g2.com/es/sellers/castor-edc)
- **Sitio web de la empresa:** www.castoredc.com
- **Año de fundación:** 2011
- **Ubicación de la sede:** New York, US
- **Twitter:** @CastorEDC  
29 seguidores en Twitter
- **Página de LinkedIn®:** [www.linkedin.com](https://www.g2.com/es/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=e3a1c7906701ea4b604fb6942ea9f3b1468c777d59192698f0b91255dbb0e2cf&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fcastoredc%2F&secure%5Burl_type%5D=linkedin_company_website)  
295 empleados en LinkedIn®

#### Who Uses This Product?

- **Top Industries:** Atención hospitalaria y sanitaria, Investigación
- **Company Size:** 48% Small, 36% Large

#### What Do G2 Reviewers Say About Castor?

_AI-generated summary from verified user reviews_

##### Pros

- Los usuarios aprecian la **facilidad de uso** de Castor, encontrándolo intuitivo y eficiente para la entrada y gestión de datos.
- Los usuarios elogian la **facilidad de navegación** de Castor, destacando su diseño amigable y el proceso sencillo de entrada de datos.
- Los usuarios elogian la **claridad y organización** de la gestión de datos de Castor, facilitando la recopilación de datos estructurados de manera efectiva.
- Los usuarios aprecian la **facilidad de diseño** de Castor, elogiando su interfaz fácil de usar y su navegación sencilla.
- Los usuarios aprecian el **progreso claro y organizado de la recopilación de datos** , capturando información en un formato estructurado.

##### Cons

- Los usuarios informan de **problemas de gestión de datos** con retrasos y notificaciones que interrumpen el proceso de entrada de datos en Castor.
- Los usuarios encuentran frustrante la función de **informes inadecuados** en Castor, ya que complica los procesos de entrada de datos y seguimiento.
- Los usuarios encuentran los **problemas de inicio de sesión** inconvenientes, ya que interrumpen el flujo de trabajo mientras ingresan datos durante las tareas clínicas.
- Los usuarios encuentran la **navegación confusa** , especialmente en lo que respecta a la gestión de consultas y el seguimiento de resoluciones pendientes.
- Los usuarios experimentan **rendimiento lento** al guardar datos y encontrar consultas resueltas, lo que afecta la usabilidad general.

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

**["El sitio está limpio y no demasiado ocupado."](https://www.g2.com/es/survey_responses/castor-review-11302811)**

**Rating:** 4.0/5.0 stars

_— Susan M._

[Read full review](https://www.g2.com/es/survey_responses/castor-review-11302811)

**["La base de datos más agradable que uso día a día."](https://www.g2.com/es/survey_responses/castor-review-11266497)**

**Rating:** 4.0/5.0 stars

_— Jessica F._

[Read full review](https://www.g2.com/es/survey_responses/castor-review-11266497)

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

- [¿Para qué se utiliza Castor EDC?](https://www.g2.com/es/discussions/what-is-castor-edc-used-for)

### [iMednet EDC](https://www.g2.com/products/imednet-edc/reviews)

Mednet, a CRScube company, is a leading healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for over 25 years to deliver the technology innovation, experience and reliability they need for success. Mednet’s comprehensive, EDC-centric eClinical platform, iMednet, optimizes clinical studies of all types and sizes – accelerating research with exceptional flexibility, ease-of-use, robust functionality, affordability, and stellar support. iMednet is feature-rich and uniquely designed to help sponsors and CROs get studies up and running quickly and to see them through with a full suite of native capabilities, including: RTSM, CTMS, eTMF, adjudication, ePRO, eConsent, payments, DICOM Imaging, RBQM, and Safety. All backed by a highly tenured and experienced support team, ensuring quality, compliance and easy onboarding of the entire research team and clinical trials sites.

**Average Rating:** 4.9/5.0

**Total Reviews:** 15

#### How Do G2 Users Rate iMednet EDC?

- **Data Capture - Electronic Data Capture (EDC):** 9.5/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 9.4/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 9.0/10 (Category avg: 8.8/10)
- **Quality of Support:** 9.8/10 (Category avg: 8.6/10)

#### Who Is the Company Behind iMednet EDC?

- **Seller:** [Mednet, a CRScube company](https://www.g2.com/sellers/mednet-a-crscube-company)
- **Year Founded:** 2001
- **HQ Location:** Minnetonka, Minnesota, USA 
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=59219795cfa924201be8dfc21d228b9b50b279c1b9f9180b91095394b4537da1&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fmednet-solutions%2F&secure%5Burl_type%5D=linkedin_company_website)  
90 employees on LinkedIn®

#### Who Uses This Product?

- **Top Industries:** Medical Devices
- **Company Size:** 47% Medium, 47% Small

#### What Do G2 Reviewers Say About iMednet EDC?

_AI-generated summary from verified user reviews_

##### Pros

- Users value the **comprehensive functionality** of iMednet EDC, supporting a wide range of clinical data management tasks.
- Users find iMednet EDC to be **very user friendly** and appreciate its organized, all-in-one module system.
- Users appreciate the **comprehensive E-Learning capabilities** of iMednet EDC, enabling a seamless learning experience across modules.
- Users value the **strong data security** features of iMednet EDC, ensuring robust protection of sensitive information.
- Users appreciate the **design ease** of iMednet EDC, finding it user-friendly and well-organized with multiple modules.

##### Cons

- Users struggle with **login issues** , needing separate credentials for each client, complicating access and workflow.
- Users find iMednet EDC's **poor navigation** challenging, particularly for those unfamiliar with the system.

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

**["Best EDC for MedTech studies"](https://www.g2.com/survey_responses/imednet-edc-review-11205801)**

**Rating:** 5.0/5.0 stars

_— Richard V._

[Read full review](https://www.g2.com/survey_responses/imednet-edc-review-11205801)

**["Good customer service and interactive database build process"](https://www.g2.com/survey_responses/imednet-edc-review-11332685)**

**Rating:** 4.0/5.0 stars

_— Sheila S. S._

[Read full review](https://www.g2.com/survey_responses/imednet-edc-review-11332685)

### [REDCap](https://www.g2.com/es/products/redcap/reviews)

REDCap es una aplicación web segura para construir y gestionar encuestas y bases de datos en línea. Aunque REDCap se puede utilizar para recopilar prácticamente cualquier tipo de datos en cualquier entorno (incluyendo el cumplimiento con 21 CFR Parte 11, FISMA, HIPAA y GDPR), está específicamente orientado a apoyar la captura de datos en línea y fuera de línea para estudios de investigación y operaciones. El Consorcio REDCap, una vasta red de apoyo de colaboradores, está compuesto por miles de socios institucionales activos en más de cien países que utilizan y apoyan sus propios sistemas REDCap individuales.

**Average Rating:** 4.3/5.0

**Total Reviews:** 214

#### How Do G2 Users Rate REDCap?

- **Captura de datos - Captura electrónica de datos (EDC):** 9.4/10 (Category avg: 8.9/10)
- **Cumplimiento - Captura electrónica de datos (EDC):** 9.1/10 (Category avg: 8.7/10)
- **eCRFs - Captura Electrónica de Datos (EDC):** 9.3/10 (Category avg: 8.8/10)
- **Calidad del soporte:** 8.2/10 (Category avg: 8.6/10)

#### Who Is the Company Behind REDCap?

- **Vendedor:** [REDCap](https://www.g2.com/es/sellers/redcap)
- **Año de fundación:** 2004
- **Ubicación de la sede:** Nashville, Tennessee
- **Página de LinkedIn®:** [www.linkedin.com](https://www.g2.com/es/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=00f4821f64e3f5a7154e5cdd1f24dd74aa89702dd13c03ca7d0eb472a956629d&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fprojectredcap%2F&secure%5Burl_type%5D=linkedin_company_website)  
72 empleados en LinkedIn®

#### Who Uses This Product?

- **Who Uses This:** Asistente de Investigación, Coordinador de Investigación
- **Top Industries:** Atención hospitalaria y sanitaria, Investigación
- **Company Size:** 62% Large, 19% Small

#### What Do G2 Reviewers Say About REDCap?

_AI-generated summary from verified user reviews_

##### Pros

- Los usuarios aprecian la **interfaz fácil de usar** de REDCap, lo que permite una coordinación y gestión de datos eficiente para fines de investigación.
- Los usuarios valoran la **interfaz fácil de usar** de REDCap, lo que permite una fácil coordinación de datos y una rápida incorporación de miembros del equipo.
- Los usuarios valoran la **interfaz fácil de usar** de REDCap, permitiendo una rápida adaptación para una coordinación de datos y una investigación eficiente.
- Los usuarios valoran la **interfaz intuitiva** de REDCap, lo que permite un aprendizaje rápido y una coordinación de investigación eficiente.

##### Cons

- Los usuarios a menudo enfrentan **rendimiento lento** con REDCap, especialmente al cargar formularios para proyectos grandes, lo que causa inconvenientes.

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

**["Rápido, fiable y fácil de usar EDC con informes sencillos"](https://www.g2.com/es/survey_responses/redcap-review-12878199)**

**Rating:** 5.0/5.0 stars

_— Pratik kadam K._

[Read full review](https://www.g2.com/es/survey_responses/redcap-review-12878199)

**["Rico en funciones y versátil para casi cualquier proyecto de datos"](https://www.g2.com/es/survey_responses/redcap-review-12264013)**

**Rating:** 5.0/5.0 stars

_— Usuario verificado en Investigación_

[Read full review](https://www.g2.com/es/survey_responses/redcap-review-12264013)

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

- [¿Para qué se utiliza REDCap?](https://www.g2.com/es/discussions/redcap-what-is-redcap-used-for)
- [Is REDCap easy to use?](https://www.g2.com/es/discussions/is-redcap-easy-to-use)
- [What is a REDCap survey?](https://www.g2.com/es/discussions/what-is-a-redcap-survey)
- [Is red cap free?](https://www.g2.com/es/discussions/is-red-cap-free)
- [What is REDCap used for?](https://www.g2.com/es/discussions/what-is-redcap-used-for)

### [Prelude EDC](https://www.g2.com/products/prelude-edc/reviews)

Prelude is the only R&D platform built exclusively for animal health and nutrition. Purpose-built for the complexity of animal studies, it gives sites and investigators the industry's most flexible, user-friendly EDC, and automates 90%+ of data management work. Founded in 2003, Prelude built one of the first eSource/EDC systems designed for complex studies without sacrificing a clean, simple experience for sites and investigators. Today it's a full eClinical platform includes: EDC, ePRO, eConsent, RTSM, and medical coding. Prelude is trusted globally by leading institutions including Cornell, Johns Hopkins, Merck, and Boehringer Ingelheim. What sets Prelude apart is partnership: fully in-house support and a configurable platform, with Customer Success Managers who work as an extension of your team through build and beyond.

**Average Rating:** 4.9/5.0

**Total Reviews:** 21

#### How Do G2 Users Rate Prelude EDC?

- **Data Capture - Electronic Data Capture (EDC):** 9.7/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 9.7/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 9.7/10 (Category avg: 8.8/10)
- **Quality of Support:** 9.9/10 (Category avg: 8.6/10)

#### Who Is the Company Behind Prelude EDC?

- **Seller:** [Prelude](https://www.g2.com/sellers/prelude)
- **Year Founded:** 2003
- **HQ Location:** Austin, TX
- **Twitter:** @PreludeEDC  
65 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=4bc0b981a8f36ceba78695b822d3015d1be430e554b7cb79737341703c1227c6&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fpreludedynamics&secure%5Burl_type%5D=linkedin_company_website)  
48 employees on LinkedIn®

#### Who Uses This Product?

- **Top Industries:** Research, Veterinary
- **Company Size:** 57% Small, 33% Medium

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

**["The only EDC that matters!"](https://www.g2.com/survey_responses/prelude-edc-review-9237084)**

**Rating:** 5.0/5.0 stars

_— Annie P._

[Read full review](https://www.g2.com/survey_responses/prelude-edc-review-9237084)

**["Director Clinical Development"](https://www.g2.com/survey_responses/prelude-edc-review-6791497)**

**Rating:** 5.0/5.0 stars

_— Jacky M._

[Read full review](https://www.g2.com/survey_responses/prelude-edc-review-6791497)

### [OpenClinica](https://www.g2.com/products/openclinica/reviews)

The OpenClinica Enterprise Edition is an enhanced, fully-supported build that is ideal for mission-critical settings.

**Average Rating:** 4.2/5.0

**Total Reviews:** 24

#### How Do G2 Users Rate OpenClinica?

- **Data Capture - Electronic Data Capture (EDC):** 8.7/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 8.3/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 8.8/10 (Category avg: 8.8/10)
- **Quality of Support:** 8.3/10 (Category avg: 8.6/10)

#### Who Is the Company Behind OpenClinica?

- **Seller:** [OpenClinica](https://www.g2.com/sellers/openclinica)
- **Year Founded:** 2004
- **HQ Location:** Waltham, Massachusetts
- **Twitter:** @OpenClinica  
1,924 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=b45c70ef2fda52be61f3c81d35bcfd01c5ec527f54358b93065a585bcdead455&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F2294775%2F&secure%5Burl_type%5D=linkedin_company_website)  
73 employees on LinkedIn®

#### Who Uses This Product?

- **Top Industries:** Research
- **Company Size:** 46% Small, 29% Medium

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

**["OpenClinica use for Investigator led Clinical Trials in the UK"](https://www.g2.com/survey_responses/openclinica-review-9339667)**

**Rating:** 5.0/5.0 stars

_— Verified User in Research_

[Read full review](https://www.g2.com/survey_responses/openclinica-review-9339667)

**["OC4 for Oncology Trials"](https://www.g2.com/survey_responses/openclinica-review-7513043)**

**Rating:** 4.5/5.0 stars

_— Verified User in Research_

[Read full review](https://www.g2.com/survey_responses/openclinica-review-7513043)

### [Drug Safety Triager](https://www.g2.com/products/drug-safety-triager/reviews)

Drug Safety Triager is our GxP validated and audit-ready pharmacovigilance (PV) literature review software solution, created from the ground up to monitor literature for Individual Case Safety Reporting, Aggregate Reports and Signal detection. It makes the drug safety literature monitoring process more efficient, cost-effective and compliant. Using intelligent automation from our machine learning engine DELVE (part of the Dialog platform) and integration with upstream and downstream processes, Drug Safety Triager takes literature reviewing to a new level. It simplifies the process so that the review teams can focus on what matters most: patient safety.

**Average Rating:** 4.5/5.0

**Total Reviews:** 15

#### How Do G2 Users Rate Drug Safety Triager?

- **Data Capture - Electronic Data Capture (EDC):** 9.2/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 9.2/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 9.2/10 (Category avg: 8.8/10)
- **Quality of Support:** 8.3/10 (Category avg: 8.6/10)

#### Who Is the Company Behind Drug Safety Triager?

- **Seller:** [Dialog Solutions](https://www.g2.com/sellers/dialog-solutions-93c463c4-a518-410e-bbde-65bb1cdd2c9d)
- **Year Founded:** 1972
- **HQ Location:** London, GB
- **Twitter:** @DialogSols  
291 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=cc1be7b7c9df0f98ef55c07a65c1bca5f859b0599c241613b03ab55ab2acb271&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F222088&secure%5Burl_type%5D=linkedin_company_website)  
47 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 40% Medium, 33% Small

#### What Are Recent G2 Reviews of Drug Safety Triager?

**["Drug safety triager: one stop solution for all PV literature needs!!"](https://www.g2.com/survey_responses/drug-safety-triager-review-8403825)**

**Rating:** 5.0/5.0 stars

_— Dr. Seema S._

[Read full review](https://www.g2.com/survey_responses/drug-safety-triager-review-8403825)

**["I would honestly use this for myself only if we didn't adopt this software."](https://www.g2.com/survey_responses/drug-safety-triager-review-7283754)**

**Rating:** 5.0/5.0 stars

_— sheena c._

[Read full review](https://www.g2.com/survey_responses/drug-safety-triager-review-7283754)

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

An award-winning, AI-native Electronic Data Capture platform Clinion EDC is built on a native AI foundation, enabling faster study builds, more efficient data review, and quicker database lock. As part of a unified eClinical platform, it ensures seamless data flow across modules while maintaining high standards of data quality and compliance. Key Capabilities: ● Accelerated Study Setup with Standardized Libraries Configure and deploy studies in weeks using prebuilt, CDASH-compliant templates. Remove manual programming with a flexible, codeless setup. ● AI-Driven Data Review and Discrepancy Detection AI reads protocol and CRF context to identify discrepancies and generate queries directly within the EDC, reducing manual review effort. ● Real-Time Mid-Study Changes Apply protocol amendments without downtime. Update forms or visits in live studies with automatic version control and no data loss. ● AI-Powered Reporting Generate custom reports using natural language inputs. Maintain audit trails and automate report sharing without coding. ● Automated CDISC/CDASH Mapping Map variables to standards within minutes using AI-assisted suggestions, reducing manual effort and supporting compliance. ● AI Assistant for In-Platform Support Access instant guidance through a conversational assistant trained on study protocols and system workflows. ● Unified Platform with Seamless Integration Works natively with RTSM, ePRO, CTMS, eConsent, and eSource, ensuring consistent data across the study lifecycle. Impact: 1–2 week average study go-live timeline 40–50% faster database lock Up to 50% reduction in study build effort Reduced manual queries and review cycles

**Average Rating:** 4.6/5.0

**Total Reviews:** 36

#### How Do G2 Users Rate Clinion EDC?

- **Data Capture - Electronic Data Capture (EDC):** 9.4/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 9.2/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 9.4/10 (Category avg: 8.8/10)
- **Quality of Support:** 9.6/10 (Category avg: 8.6/10)

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

- **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?

- **Top Industries:** Pharmaceuticals, Research
- **Company Size:** 49% Medium, 43% Small

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

**["USER FRIENDLY EDC TOOL"](https://www.g2.com/survey_responses/clinion-edc-review-9633197)**

**Rating:** 4.0/5.0 stars

_— Jenish E._

[Read full review](https://www.g2.com/survey_responses/clinion-edc-review-9633197)

**["Clinion- "The user Friendly EDC""](https://www.g2.com/survey_responses/clinion-edc-review-9129671)**

**Rating:** 4.0/5.0 stars

_— Dr. Sahaja K._

[Read full review](https://www.g2.com/survey_responses/clinion-edc-review-9129671)

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

- [What is Clinion EDC used for?](https://www.g2.com/discussions/what-is-clinion-edc-used-for) - 1 comment

### [Clinical Research Suite](https://www.g2.com/es/products/clinical-research-suite/reviews)

ACERCA DE ResearchManager es una plataforma todo en uno que hace que la investigación clínica sea más inteligente, rápida y eficiente. Con el Clinical Research Suite, proporcionamos una solución totalmente integrada para instituciones académicas, organizaciones de salud, CROs y patrocinadores a lo largo de todo el ciclo de vida de la investigación clínica. Desde la configuración del estudio y la aprobación regulatoria hasta el reclutamiento, la captura de datos y el monitoreo. Al centralizar procesos y datos en una sola plataforma, ResearchManager reduce la complejidad, minimiza errores y mejora el cumplimiento y la colaboración. NUESTRA MISIÓN Nuestra misión es digitalizar, acelerar y optimizar la investigación en todo el mundo, permitiendo que tratamientos innovadores y conocimientos científicos lleguen a los pacientes más pronto. Creemos que avanzar en la atención médica comienza con avanzar en la investigación, y empoderamos a las organizaciones para que eso suceda. NUESTRA PLATAFORMA - EL CLINICAL RESEARCH SUITE Gestión de Datos Clínicos: Herramientas para reclutar a los participantes adecuados y capturar, gestionar y validar datos de investigación de manera eficiente, reduciendo errores y ahorrando tiempo. • Captura Electrónica de Datos (EDC) • Resultados Electrónicos Informados por el Paciente (ePRO) • Gestión de Aleatorización y Suministro de Ensayos (RTSM) • Consentimiento Informado Electrónico (eConsent) • Reclutamiento de Pacientes Operaciones Clínicas: Herramientas que centralizan las presentaciones, documentación y flujos de trabajo para agilizar la gestión de ensayos y fortalecer la colaboración. Todas son modulares y totalmente configurables. • Sistema de Gestión de Ensayos Clínicos (CTMS) • Archivo Maestro Electrónico de Ensayos (eTMF) • Sistema de Gestión de Información Regulatoria (RIMS) APRENDE MÁS • Solicita una DEMO GRATIS: https://my-researchmanager.com/en/request-inquiry/ • Obtén una Estimación de Precio en 1 Minuto: https://my-researchmanager.com/en/pricing/

**Average Rating:** 3.8/5.0

**Total Reviews:** 204

#### How Do G2 Users Rate Clinical Research Suite?

- **Captura de datos - Captura electrónica de datos (EDC):** 7.6/10 (Category avg: 8.9/10)
- **Cumplimiento - Captura electrónica de datos (EDC):** 7.9/10 (Category avg: 8.7/10)
- **eCRFs - Captura Electrónica de Datos (EDC):** 7.7/10 (Category avg: 8.8/10)
- **Calidad del soporte:** 7.6/10 (Category avg: 8.6/10)

#### Who Is the Company Behind Clinical Research Suite?

- **Vendedor:** [ResearchManager](https://www.g2.com/es/sellers/researchmanager)
- **Año de fundación:** 2013
- **Ubicación de la sede:** Deventer, Overijssel
- **Twitter:** @RESEARCH\_MGR  
96 seguidores en Twitter
- **Página de LinkedIn®:** [www.linkedin.com](https://www.g2.com/es/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=bb0174c3c2958e513e4df01be8316114b84868159612f408197f37a7f8109c6f&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fresearch-manager%2F&secure%5Burl_type%5D=linkedin_company_website)  
20 empleados en LinkedIn®

#### Who Uses This Product?

- **Who Uses This:** Estudiante de doctorado, Investigador
- **Top Industries:** Atención hospitalaria y sanitaria, Investigación
- **Company Size:** 55% Large, 33% Small

#### What Do G2 Reviewers Say About Clinical Research Suite?

_AI-generated summary from verified user reviews_

##### Pros

- Los usuarios aprecian la **interfaz fácil de usar** de Clinical Research Suite, mejorando su experiencia con una estructura y organización claras.
- Los usuarios aprecian la **claridad de la interfaz** de Clinical Research Suite, destacando su clara organización y facilidad de uso.
- Los usuarios valoran la **interfaz fácil de usar** que mejora la navegación y la organización, agilizando los procesos de investigación de manera efectiva.
- Los usuarios aprecian las **funciones fáciles de navegar** de Clinical Research Suite, mejorando su experiencia y eficiencia general.
- Los usuarios aprecian la **gestión eficiente de datos** en Clinical Research Suite, asegurando cargas de estudio seguras y organizadas.

##### Cons

- Los usuarios encuentran la **pobre navegación** de la Suite de Investigación Clínica frustrante y que consume mucho tiempo, complicando su experiencia general.
- Los usuarios encuentran que las **características faltantes** como la personalización y las guías detalladas obstaculizan la experiencia general de Clinical Research Suite.
- Los usuarios enfrentan una **curva de aprendizaje pronunciada** con el Conjunto de Investigación Clínica, lo que complica la navegación inicial y la comprensión de los requisitos.
- Los usuarios encuentran **frustrante el rendimiento lento** del Conjunto de Investigación Clínica, especialmente al gestionar grandes conjuntos de datos.
- Los usuarios luchan con **problemas de gestión de datos** ya que las cargas de documentos conducen a la desorganización y la pérdida de supervisión.

#### What Are Recent G2 Reviews of Clinical Research Suite?

**["Interfaz de usuario muy amigable"](https://www.g2.com/es/survey_responses/clinical-research-suite-review-11695059)**

**Rating:** 4.5/5.0 stars

_— Usuario verificado en Práctica médica_

[Read full review](https://www.g2.com/es/survey_responses/clinical-research-suite-review-11695059)

**["Software muy flexible"](https://www.g2.com/es/survey_responses/clinical-research-suite-review-10816362)**

**Rating:** 5.0/5.0 stars

_— Quinty v._

[Read full review](https://www.g2.com/es/survey_responses/clinical-research-suite-review-10816362)

### [TrialKit](https://www.g2.com/products/trialkit/reviews)

TrialKit is a unified eClinical platform designed to simplify and streamline data collection and study management in clinical research. This end-to-end solution caters to the needs of sponsors, CROs, and clinical sites by providing a suite of tools that includes electronic data capture (EDC), electronic patient-reported outcomes (ePRO), electronic clinical outcome assessments (eCOA), eConsent, medical coding, AI study intelligence, and more. With its web-based interface and a native mobile app, TrialKit allows users to securely collect, manage, and analyze study data from virtually anywhere, enhancing the flexibility and accessibility of clinical research. Targeted at clinical researchers and organizations conducting studies of varying sizes and complexities, TrialKit is particularly beneficial for those looking to expedite their research processes without sacrificing compliance or data integrity. The platform’s intuitive drag-and-drop form builder enables users to create and deploy regulatory-compliant studies quickly, eliminating the need for extensive programming knowledge. This feature has made TrialKit a preferred choice for over 9,000 studies across diverse therapeutic areas, showcasing its adaptability and user-friendly design. A core differentiator of the platform is TrialKit AI, recognized with the 2024 SCDM Innovation Award for Health Technology Solutions. TrialKit AI extends the platform with embedded intelligence, enabling teams to go beyond traditional reporting and analytics. Capabilities include protocol design/ingestion, study design, study build, simulation, validation, and advanced analysis—allowing users to model study outcomes, evaluate design decisions, and identify risks earlier in the trial lifecycle. TrialKit AI can also ingest external datasets, providing a broader foundation for analysis and enabling more informed, data-driven decisions across studies. By embedding these capabilities directly within the platform, TrialKit AI supports faster insights, more efficient study execution, and improved decision-making without requiring separate systems or tools. This integrated approach reduces operational complexity while enhancing the ability of research teams to proactively manage study performance. TrialKit’s emphasis on unified workflows and operational efficiency translates into meaningful cost savings for organizations. By centralizing data collection, management, and analysis within a single platform, TrialKit reduces reliance on fragmented systems and minimizes manual processes. As clinical research continues to evolve, TrialKit provides a flexible and scalable solution that supports modern study designs while maintaining a strong foundation in data integrity, compliance, and usability.

**Average Rating:** 4.6/5.0

**Total Reviews:** 24

#### How Do G2 Users Rate TrialKit?

- **Data Capture - Electronic Data Capture (EDC):** 9.0/10 (Category avg: 8.9/10)
- **Compliance - Electronic Data Capture (EDC):** 9.0/10 (Category avg: 8.7/10)
- **eCRFs - Electronic Data Capture (EDC):** 9.1/10 (Category avg: 8.8/10)
- **Quality of Support:** 9.3/10 (Category avg: 8.6/10)

#### Who Is the Company Behind TrialKit?

- **Seller:** [Crucial Data Solutions](https://www.g2.com/sellers/crucial-data-solutions)
- **Year Founded:** 2010
- **HQ Location:** Reno
- **Twitter:** @Crucial\_Data  
286 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=25ae58dfbb30b40db84caf8c149d1aff6b8f21de857ac23d3c9a94cf6a9ad4b2&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fcrucial-data-solutions-inc%2F&secure%5Burl_type%5D=linkedin_company_website)  
16 employees on LinkedIn®

#### Who Uses This Product?

- **Top Industries:** Medical Devices
- **Company Size:** 58% Small, 35% Medium

#### What Do G2 Reviewers Say About TrialKit?

_AI-generated summary from verified user reviews_

##### Pros

- Users commend the **exceptional customer support** from TrialKit, noting their responsiveness and attentiveness to needs.
- Users find TrialKit's **ease of use** impressive, emphasizing the platform's intuitive design and supportive team.
- Users appreciate the **comprehensive features** of TrialKit, including great UI and exceptional customer support.
- Users commend the **excellent user interface** of TrialKit, facilitating ease of navigation and usage across the platform.
- Users value the **access ease** of TrialKit, enabling quick adjustments and seamless integration during form building.

##### Cons

- Users find the **documentation difficult** , leading to confusion about settings and cumbersome reporting functionality.
- Users find the **inadequate reporting** in TrialKit to be cumbersome and time-consuming for capturing key metrics.
- Users find the **sales to study development process unclear** , leading to delays and frustrations in using TrialKit.
- Users feel there is **limited flexibility** in customizing the dashboard and homepage, impacting their experience with TrialKit.
- Users experience **slow performance** with TrialKit, citing delays, bugs, and heavy costs associated with its use.

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

**["Effortless Data Management and Outstanding Support"](https://www.g2.com/survey_responses/trialkit-review-11968980)**

**Rating:** 4.0/5.0 stars

_— Roberta H._

[Read full review](https://www.g2.com/survey_responses/trialkit-review-11968980)

**["An experiment for a non-standard use case"](https://www.g2.com/survey_responses/trialkit-review-12237697)**

**Rating:** 4.0/5.0 stars

_— Kathryn S._

[Read full review](https://www.g2.com/survey_responses/trialkit-review-12237697)

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 ![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 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

Show More

* * *

## 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. 

### 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. 

**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. 

**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. 

**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. 

**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. 

**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&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. 

**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.