Veeva Clinical Platform

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

Company Name

Veeva

Product URL

https://www.veeva.com/products/veeva-clinical-platform/

Company URL

https://www.veeva.com

Categories

• clinical Operations
• clinical Data Management
• patient Engagement

Summary

Veeva Clinical Platform is a unified cloud-based suite designed to streamline and standardize clinical trials, enhancing efficiency for sponsors, simplifying processes for sites, and improving patient engagement through a connected experience.

Description

Veeva Clinical Platform offers a comprehensive set of applications that unify clinical operations and data management. It includes solutions for clinical operations, clinical data management, and patient engagement, all integrated to accelerate study timelines and improve collaboration among sponsors, sites, and patients.

Api Available

yes

Certifications

• ISO 27001
• ISO 27018
• SOC 1 Type II
• SOC 2 Type II
• EU-U.S. and Swiss-U.S. Privacy Shield Frameworks
• ISO 9001
• ISO 22301
• ISO 27017
• ISO 20000-1
• ISO 27035
• ISO 27036
• ISO 27037
• ISO 27039
• ISO 27041
• ISO 27042
• ISO 27043
• ISO 27044
• ISO 27045
• ISO 27046

Company Founding

2007

Company Offices

• United States
• Germany
• France
• United Kingdom
• China
• Japan
• South Korea
• Brazil
• Mexico
• India

Compliance

• HIPAA
• GDPR
• 21 CFR Part 11
• ISO 27001
• SOC 2 Type II
• ISO 27018
• SOC 1 Type II
• EU Annex 11
• CCPA
• CPRA

Customers

• Parexel
• University's pharmaceutical product development and research division
• Pharmaceuticals
• Enterprise (> 1000 emp.)
• Mid-Market (51-1000 emp.)

Data Residency

Multiple regions including North America, Europe, and Asia Pacific

Data Standards

• HL7 FHIR
• E2B
• CDISC SDTM
• CDISC ADaM
• LOINC
• MedDRA
• WHODrug

Deployment Model

• SaaS

Features

• Clinical Operations
• Clinical Data Management
• Clinical Research Sites Management
• Patient Engagement
• Clinical Trial Management
• Electronic Trial Master File (eTMF)
• Clinical Trial Management System (CTMS)
• Clinical Data Repository (CDB)
• Electronic Data Capture (EDC)
• Clinical Trial Payments
• Study Startup
• Site Connect
• Study Training
• Disclosures
• OpenData Clinical
• Randomization and Supply Management (RTSM)
• Electronic Clinical Outcome Assessment (eCOA)

Id

SW2774

Integration Partners

• Salesforce

Integrations

• Veeva EDC
• Veeva CTMS
• Veeva CDB
• Veeva eCOA
• Veeva SiteVault
• Veeva OpenData Clinical
• Veeva Study Training
• Veeva Disclosures
• Veeva Payments
• Veeva Study Startup
• Veeva Site Connect
• Veeva RTSM
• Veeva MyVeeva for Patients
• Veeva Vault Platform
• Veeva AI Agents
• Veeva Connections Hub
• Veeva CRM Suite
• Veeva Vault Regulatory
• Veeva Vault Quality
• Veeva Vault Safety Suite

Languages Supported

• English
• German
• Spanish
• French
• Italian
• Chinese
• Japanese
• Korean
• Portuguese

Last Updated

2025-10-11

License

commercial

Market Segment

• enterprise
• smb

Optional Modules

• Veeva AI Agents
• Veeva Vault Platform

Os Platforms

• Web
• iOS
• Android

Pricing Details

Contact vendor for pricing information.

Pricing Model

subscription

Privacy Features

• Business Associate Agreement (BAA)
• Consent Management
• Data Anonymization
• Data Minimization
• Data Masking
• Data Encryption
• Access Controls
• Data Retention Policies
• Data Subject Rights Management
• Privacy Impact Assessments

Product Code

SW2774

Product Name

Veeva Clinical Platform

Ratings

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

Regions Available

• North America
• Europe
• Asia Pacific
• Latin America

Related Urls

Release Year

2012

Security Features

• Encryption
• Role-Based Access Control (RBAC)
• Single Sign-On (SSO)
• Audit Logs
• Two-Factor Authentication (2FA)
• Data Loss Prevention (DLP)
• Intrusion Detection Systems (IDS)
• Firewalls
• Network Segmentation
• Regular Security Audits

Specialties

• Clinical Trials
• Clinical Data Management
• Patient Engagement

Support Channels

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

System Requirements

Target Users

• sponsors
• clinical research organizations (CROs)
• clinical research sites
• patients

Training Options

• documentation
• webinars
• live_online
• onsite
• certification

Type

product

User Reviews

• Incredible software. It's valuable and important software to store and reference the documents. It's built nature and updations are superb.
• I like that most pharma and biotech companies use this product so that there is an easy integration process. Overall, Veeva Vault QMS is easy to use and makes storing documents and associated files a breeze.
• I like the factor how Veeva vault turned the documentation part easy and trackable for us.
• Excellent support and ease of use. Seamless release management and GxP compliance.
• Interface friendly and the availability of support options. Organized database.
• Provides E2E Regulatory Activities oversight solution with a clear audit trail. Also possesses ability to integrate with other cloud tools.
• A very secure platform that allows tracking of reviews for research documents and standard operating protocols. It helps assign new hires tasks to read and understand documents and complete their training.
• Makes continuous workflows very well automated. Very helpful to maintain GxP compliance.
• Best platform for document management, it integrates quality assurance and regulatory compliance requirements. It applies a lifecycle to each document, especially useful for ones that need a routine update. And there is no need for a third-party signature tool, Veeva allows document approval or other authorizations within the system.
• Working with the Veeva implementation team has been a pleasure. The application is intuitively designed and well built. I would recommend Veeva to anyone looking to implement a CRM solution. They are industry leaders and well versed in industry challenges.
• Great vertical, offering a lot of out of the box solutions, but also gives IT the ability to customize the solution to cater to specific market demands. Built on Salesforce, it also integrates well with other applications.

Version

1.0

Alternatives

See related products

Canonical JSON

{
  "product_name": "Veeva Clinical Platform",
  "company_name": "Veeva",
  "product_url": "https://www.veeva.com/products/veeva-clinical-platform/",
  "company_url": "https://www.veeva.com",
  "related_urls": [],
  "product_code": "SW2774",
  "summary": "Veeva Clinical Platform is a unified cloud-based suite designed to streamline and standardize clinical trials, enhancing efficiency for sponsors, simplifying processes for sites, and improving patient engagement through a connected experience.",
  "description": "Veeva Clinical Platform offers a comprehensive set of applications that unify clinical operations and data management. It includes solutions for clinical operations, clinical data management, and patient engagement, all integrated to accelerate study timelines and improve collaboration among sponsors, sites, and patients.",
  "categories": [
    "clinical Operations",
    "clinical Data Management",
    "patient Engagement",
    "Clinical Operations",
    "Clinical Data Management",
    "Patient Engagement"
  ],
  "market_segment": [
    "enterprise",
    "smb"
  ],
  "target_users": [
    "sponsors",
    "clinical research organizations (CROs)",
    "clinical research sites",
    "patients"
  ],
  "specialties": [
    "Clinical Trials",
    "Clinical Data Management",
    "Patient Engagement"
  ],
  "regions_available": [
    "North America",
    "Europe",
    "Asia Pacific",
    "Latin America"
  ],
  "languages_supported": [
    "English",
    "German",
    "Spanish",
    "French",
    "Italian",
    "Chinese",
    "Japanese",
    "Korean",
    "Portuguese"
  ],
  "pricing_model": "subscription",
  "pricing_details": "Contact vendor for pricing information.",
  "license": "commercial",
  "company_offices": [
    "United States",
    "Germany",
    "France",
    "United Kingdom",
    "China",
    "Japan",
    "South Korea",
    "Brazil",
    "Mexico",
    "India"
  ],
  "company_founding": "2007",
  "deployment_model": [
    "SaaS"
  ],
  "os_platforms": [
    "Web",
    "iOS",
    "Android"
  ],
  "features": [
    "Clinical Operations",
    "Clinical Data Management",
    "Clinical Research Sites Management",
    "Patient Engagement",
    "Clinical Trial Management",
    "Electronic Trial Master File (eTMF)",
    "Clinical Trial Management System (CTMS)",
    "Clinical Data Repository (CDB)",
    "Electronic Data Capture (EDC)",
    "Clinical Trial Payments",
    "Study Startup",
    "Site Connect",
    "Study Training",
    "Disclosures",
    "OpenData Clinical",
    "Randomization and Supply Management (RTSM)",
    "Electronic Clinical Outcome Assessment (eCOA)"
  ],
  "optional_modules": [
    "Veeva AI Agents",
    "Veeva Vault Platform"
  ],
  "integrations": [
    "Veeva EDC",
    "Veeva CTMS",
    "Veeva CDB",
    "Veeva eCOA",
    "Veeva SiteVault",
    "Veeva OpenData Clinical",
    "Veeva Study Training",
    "Veeva Disclosures",
    "Veeva Payments",
    "Veeva Study Startup",
    "Veeva Site Connect",
    "Veeva RTSM",
    "Veeva MyVeeva for Patients",
    "Veeva Vault Platform",
    "Veeva AI Agents",
    "Veeva Connections Hub",
    "Veeva CRM Suite",
    "Veeva Vault Regulatory",
    "Veeva Vault Quality",
    "Veeva Vault Safety Suite"
  ],
  "data_standards": [
    "HL7 FHIR",
    "E2B",
    "CDISC SDTM",
    "CDISC ADaM",
    "LOINC",
    "MedDRA",
    "WHODrug"
  ],
  "api_available": "yes",
  "system_requirements": "",
  "compliance": [
    "HIPAA",
    "GDPR",
    "21 CFR Part 11",
    "ISO 27001",
    "SOC 2 Type II",
    "ISO 27018",
    "SOC 1 Type II",
    "EU Annex 11",
    "CCPA",
    "CPRA"
  ],
  "certifications": [
    "ISO 27001",
    "ISO 27018",
    "SOC 1 Type II",
    "SOC 2 Type II",
    "EU-U.S. and Swiss-U.S. Privacy Shield Frameworks",
    "ISO 9001",
    "ISO 22301",
    "ISO 27017",
    "ISO 20000-1",
    "ISO 27035",
    "ISO 27036",
    "ISO 27037",
    "ISO 27039",
    "ISO 27041",
    "ISO 27042",
    "ISO 27043",
    "ISO 27044",
    "ISO 27045",
    "ISO 27046"
  ],
  "security_features": [
    "Encryption",
    "Role-Based Access Control (RBAC)",
    "Single Sign-On (SSO)",
    "Audit Logs",
    "Two-Factor Authentication (2FA)",
    "Data Loss Prevention (DLP)",
    "Intrusion Detection Systems (IDS)",
    "Firewalls",
    "Network Segmentation",
    "Regular Security Audits"
  ],
  "privacy_features": [
    "Business Associate Agreement (BAA)",
    "Consent Management",
    "Data Anonymization",
    "Data Minimization",
    "Data Masking",
    "Data Encryption",
    "Access Controls",
    "Data Retention Policies",
    "Data Subject Rights Management",
    "Privacy Impact Assessments"
  ],
  "data_residency": "Multiple regions including North America, Europe, and Asia Pacific",
  "customers": [
    "Parexel",
    "University's pharmaceutical product development and research division",
    "Pharmaceuticals",
    "Enterprise (> 1000 emp.)",
    "Mid-Market (51-1000 emp.)"
  ],
  "user_reviews": [
    "Incredible software. It's valuable and important software to store and reference the documents. It's built nature and updations are superb.",
    "I like that most pharma and biotech companies use this product so that there is an easy integration process. Overall, Veeva Vault QMS is easy to use and makes storing documents and associated files a breeze.",
    "I like the factor how Veeva vault turned the documentation part easy and trackable for us.",
    "Excellent support and ease of use. Seamless release management and GxP compliance.",
    "Interface friendly and the availability of support options. Organized database.",
    "Provides E2E Regulatory Activities oversight solution with a clear audit trail. Also possesses ability to integrate with other cloud tools.",
    "A very secure platform that allows tracking of reviews for research documents and standard operating protocols. It helps assign new hires tasks to read and understand documents and complete their training.",
    "Makes continuous workflows very well automated. Very helpful to maintain GxP compliance.",
    "Best platform for document management, it integrates quality assurance and regulatory compliance requirements. It applies a lifecycle to each document, especially useful for ones that need a routine update. And there is no need for a third-party signature tool, Veeva allows document approval or other authorizations within the system.",
    "Working with the Veeva implementation team has been a pleasure. The application is intuitively designed and well built. I would recommend Veeva to anyone looking to implement a CRM solution. They are industry leaders and well versed in industry challenges.",
    "Great vertical, offering a lot of out of the box solutions, but also gives IT the ability to customize the solution to cater to specific market demands. Built on Salesforce, it also integrates well with other applications."
  ],
  "ratings": [
    "4.2 out of 5 stars on G2",
    "4.0 out of 5 on G2"
  ],
  "support_channels": [
    "email",
    "phone",
    "chat",
    "ticketing",
    "community",
    "24x7"
  ],
  "training_options": [
    "documentation",
    "webinars",
    "live_online",
    "onsite",
    "certification"
  ],
  "release_year": "2012",
  "integration_partners": [
    "Salesforce"
  ],
  "id": "SW2774",
  "slug": "veeva-clinical-platform",
  "type": "product",
  "version": "1.0",
  "last_updated": "2025-10-11",
  "links_json": {
    "self": "https://www.healthaidb.com/software/veeva-clinical-platform.json"
  }
}