Veeva EDC

JSON twin: https://www.healthaidb.com/software/veeva-edc.json

Company Name

Veeva

Product URL

https://www.veeva.com/products/veeva-edc/

Company URL

https://www.veeva.com

Categories

• clinical Data Management
• clinical Operations
• clinical Research
• clinical Data Collection
• data Integration
• clinical Data Archiving
• Clinical Trials
• Clinical Data Capture
• Clinical Data Processing
• Clinical Data Review
• Clinical Data Integration
• Clinical Data Quality Control

Summary

Veeva EDC is a cloud-based Electronic Data Capture system designed to streamline the collection, review, and processing of clinical trial data, enhancing efficiency and agility in complex studies.

Description

Veeva EDC offers an end-to-end environment for managing clinical trial data, from designing patient forms and quality control checks during study initiation to collecting patient data, local labs, and medical coding during execution. It includes quality controls such as querying, targeted source data verification (SDV), and protocol deviations. At study completion, it provides data lock and post-processing features, including automatic end-of-study media creation and archiving. The system is built on modern cloud technologies, offering a user-friendly interface and eliminating the need for custom programming. It supports complex trial designs, including master protocols and adaptive designs, without requiring downtime for protocol amendments. Veeva EDC integrates seamlessly with other Veeva applications, facilitating bi-directional data flow and enhancing overall clinical data management. Notably, eight of the top 20 biopharmaceutical companies have standardized on Veeva EDC, underscoring its effectiveness in modernizing clinical data management processes.

Api Available

yes

Certifications

• FDA 510(k)
• CE/MDR
• ONC
• ISO 13485

Company Founding

2007

Company Offices

• United States
• Germany
• United Kingdom
• France
• Italy
• China
• Japan
• India
• Singapore
• Australia

Compliance

• HIPAA
• GDPR
• HITECH
• SOC 2
• ISO 27001

Customers

Data Residency

US/EU regions

Data Standards

• FHIR
• HL7 v2
• DICOM
• SNOMED
• ICD-10

Deployment Model

• SaaS

Features

• Visual drag-and-drop study designer
• Dynamic visits and forms
• Scripting wizard for edit checks
• Self-documenting specifications
• Real-time and risk-based user acceptance testing (UAT)
• Amendments without downtime
• Local lab data management
• DICOM image collection and viewing
• Direct access to study data
• High-volume export API
• Bi-directional data flow with Veeva applications

Id

SW2775

Integration Partners

• Medidata Rave
• Viedoc
• Florence eBinders
• Fusion eClinical Suite EDC
• Vial EDC + eSource
• ResearchManager
• Rave CTMS
• TrialHub
• TrialKit
• REDCap
• Medrio EDC
• Castor
• OpenClinica
• Egnyte
• Vodori
• Clinical Research Suite

Integrations

• Veeva Safety
• Veeva CDB
• Veeva RTSM
• Veeva CTMS
• Veeva Payments
• Veeva eTMF
• Veeva Site Connect
• Veeva Study Training
• Third-party EDCs
• RTSM systems
• eCOA systems
• Laboratory systems
• Imaging systems

Languages Supported

• English
• German
• Spanish
• French
• Italian
• Chinese
• Japanese
• Korean
• Portuguese
• Russian
• Turkish
• Arabic
• Hindi
• Bengali
• Punjabi
• Javanese
• Telugu
• Vietnamese
• Thai

Last Updated

2025-10-11

License

commercial

Market Segment

• enterprise
• smb

Optional Modules

• Veeva CDB
• Veeva eCOA
• Veeva CTMS
• Veeva Safety
• Veeva RTSM
• Veeva eTMF
• Veeva Payments
• Veeva Study Startup
• Veeva Site Connect
• Veeva Study Training

Os Platforms

• Web
• iOS
• Android

Pricing Details

Contact vendor for pricing information.

Pricing Model

subscription

Privacy Features

• Business Associate Agreement (BAA) available
• Consent management
• Anonymization
• Data minimization

Product Code

SW2775

Product Name

Veeva EDC

Ratings

• 4.2 out of 5 stars on G2
• 4.1 out of 5 stars on G2

Regions Available

• North America
• Europe
• Asia Pacific
• Latin America
• China
• Japan
• Korea
• Australia
• India
• Middle East
• Africa
• South America
• Russia
• Turkey
• Brazil
• Mexico
• Argentina
• South Korea
• Singapore
• Malaysia
• Thailand

Related Urls

Release Year

2012

Security Features

• Encryption
• Role-Based Access Control (RBAC)
• Single Sign-On (SSO)
• Audit logs
• Two-Factor Authentication (2FA)

Specialties

• Clinical Data Management
• Clinical Trial Management
• Clinical Research
• Biostatistics
• Data Analysis
• Clinical Operations
• Pharmaceutical Research
• Biotech Research
• Medical Coding
• Data Integration
• Data Quality Control
• Data Archiving
• Protocol Management
• Adaptive Trial Designs
• Cloud-based Clinical Data Systems
• Clinical Data Processing
• Clinical Data Review
• Clinical Data Capture
• Clinical Data Integration
• Clinical Data Archiving

Support Channels

• email
• phone
• chat
• ticketing
• community
• 24x7

System Requirements

Target Users

• clinical researchers
• data managers
• clinical trial managers
• biostatisticians
• clinical data coordinators
• clinical data analysts
• clinical operations teams
• clinical research organizations (CROs)
• pharmaceutical companies
• biotech companies

Training Options

• documentation
• webinars
• live_online
• onsite
• certification

Type

product

User Reviews

Version

1.0

Alternatives

See related products

Canonical JSON

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  "company_name": "Veeva",
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  "company_url": "https://www.veeva.com",
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  "description": "Veeva EDC offers an end-to-end environment for managing clinical trial data, from designing patient forms and quality control checks during study initiation to collecting patient data, local labs, and medical coding during execution. It includes quality controls such as querying, targeted source data verification (SDV), and protocol deviations. At study completion, it provides data lock and post-processing features, including automatic end-of-study media creation and archiving. The system is built on modern cloud technologies, offering a user-friendly interface and eliminating the need for custom programming. It supports complex trial designs, including master protocols and adaptive designs, without requiring downtime for protocol amendments. Veeva EDC integrates seamlessly with other Veeva applications, facilitating bi-directional data flow and enhancing overall clinical data management. Notably, eight of the top 20 biopharmaceutical companies have standardized on Veeva EDC, underscoring its effectiveness in modernizing clinical data management processes.",
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    "Latin America",
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    "Japan",
    "Korea",
    "Australia",
    "India",
    "Middle East",
    "Africa",
    "South America",
    "Russia",
    "Turkey",
    "Brazil",
    "Mexico",
    "Argentina",
    "South Korea",
    "Singapore",
    "Malaysia",
    "Thailand"
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  "languages_supported": [
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    "Italian",
    "Chinese",
    "Japanese",
    "Korean",
    "Portuguese",
    "Russian",
    "Turkish",
    "Arabic",
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    "Punjabi",
    "Javanese",
    "Telugu",
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  "pricing_model": "subscription",
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  "license": "commercial",
  "company_offices": [
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    "Germany",
    "United Kingdom",
    "France",
    "Italy",
    "China",
    "Japan",
    "India",
    "Singapore",
    "Australia"
  ],
  "company_founding": "2007",
  "deployment_model": [
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  "os_platforms": [
    "Web",
    "iOS",
    "Android"
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  "features": [
    "Visual drag-and-drop study designer",
    "Dynamic visits and forms",
    "Scripting wizard for edit checks",
    "Self-documenting specifications",
    "Real-time and risk-based user acceptance testing (UAT)",
    "Amendments without downtime",
    "Local lab data management",
    "DICOM image collection and viewing",
    "Direct access to study data",
    "High-volume export API",
    "Bi-directional data flow with Veeva applications"
  ],
  "optional_modules": [
    "Veeva CDB",
    "Veeva eCOA",
    "Veeva CTMS",
    "Veeva Safety",
    "Veeva RTSM",
    "Veeva eTMF",
    "Veeva Payments",
    "Veeva Study Startup",
    "Veeva Site Connect",
    "Veeva Study Training"
  ],
  "integrations": [
    "Veeva Safety",
    "Veeva CDB",
    "Veeva RTSM",
    "Veeva CTMS",
    "Veeva Payments",
    "Veeva eTMF",
    "Veeva Site Connect",
    "Veeva Study Training",
    "Third-party EDCs",
    "RTSM systems",
    "eCOA systems",
    "Laboratory systems",
    "Imaging systems"
  ],
  "data_standards": [
    "FHIR",
    "HL7 v2",
    "DICOM",
    "SNOMED",
    "ICD-10"
  ],
  "api_available": "yes",
  "system_requirements": "",
  "compliance": [
    "HIPAA",
    "GDPR",
    "HITECH",
    "SOC 2",
    "ISO 27001"
  ],
  "certifications": [
    "FDA 510(k)",
    "CE/MDR",
    "ONC",
    "ISO 13485"
  ],
  "security_features": [
    "Encryption",
    "Role-Based Access Control (RBAC)",
    "Single Sign-On (SSO)",
    "Audit logs",
    "Two-Factor Authentication (2FA)"
  ],
  "privacy_features": [
    "Business Associate Agreement (BAA) available",
    "Consent management",
    "Anonymization",
    "Data minimization"
  ],
  "data_residency": "US/EU regions",
  "customers": [],
  "user_reviews": [],
  "ratings": [
    "4.2 out of 5 stars on G2",
    "4.1 out of 5 stars on G2"
  ],
  "support_channels": [
    "email",
    "phone",
    "chat",
    "ticketing",
    "community",
    "24x7"
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  "training_options": [
    "documentation",
    "webinars",
    "live_online",
    "onsite",
    "certification"
  ],
  "release_year": "2012",
  "integration_partners": [
    "Medidata Rave",
    "Viedoc",
    "Florence eBinders",
    "Fusion eClinical Suite EDC",
    "Vial EDC + eSource",
    "ResearchManager",
    "Rave CTMS",
    "TrialHub",
    "TrialKit",
    "REDCap",
    "Medrio EDC",
    "Castor",
    "OpenClinica",
    "Egnyte",
    "Vodori",
    "Clinical Research Suite"
  ],
  "id": "SW2775",
  "slug": "veeva-edc",
  "type": "product",
  "version": "1.0",
  "last_updated": "2025-10-11",
  "links_json": {
    "self": "https://www.healthaidb.com/software/veeva-edc.json"
  }
}