Medidata Link

JSON twin: https://www.healthaidb.com/software/medidata-link.json

Company Name

Medidata

Product URL

https://www.medidata.com/en/clinical-trial-products/medidata-ai/real-world-data/link-real-world-and-clinical-trial-data/

Company URL

https://www.medidata.com

Categories

• clinical Data Management
• data Platform
• data Privacy
• Health Data Platforms
• Patient Data Tokenization

Summary

Medidata Link is a data integration platform that connects clinical trial data with real-world data at the patient level to enhance evidence generation and patient outcomes.

Description

Medidata Link enables the linkage of patient-level clinical trial data with real-world data (RWD) to provide a comprehensive view of the patient journey before, during, and after clinical trials. This integration supports long-term follow-up, reduces patient loss to follow-up, and facilitates the creation of external control arms, thereby accelerating access to innovative treatments while minimizing site burden and costs. The platform is fully integrated with the Medidata Unified Platform and supports various consent models, including paper and eConsent, ensuring seamless data collection across multiple research sites. It also offers pre-built integrations with tokenization technology partners and connects to a broad ecosystem of RWD sources, facilitating secure and compliant data linkage. Medidata Link is designed to be agnostic of consent methods and protects sponsors from the risks associated with directly holding personally identifiable information (PII) by streamlining third-party data privacy certifications. This approach allows sponsors to collect trial data and connect it to patients' RWD, bridging evidence gaps and enhancing confidence in clinical decision-making. The solution is part of Medidata's broader suite of clinical trial products, which aim to optimize clinical trial design, planning, and execution through AI-powered analytics and seamless integration.

Api Available

yes

Certifications

• FDA 510(k)
• CE/MDR
• ONC
• ISO 27001
• ISO 27017
• ISO 27018
• ISO 27701

Company Founding

1999

Company Offices

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

Compliance

• HIPAA
• GDPR
• HITECH
• SOC 2
• ISO 27001
• ISO 27017
• ISO 27018
• ISO 27701

Customers

Data Residency

US/EU regions

Data Standards

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

Deployment Model

• SaaS

Features

• Connects patient-level clinical trial data with real-world data (RWD)
• Enables longitudinal patient tracking before, during, and after clinical trials
• Supports monitoring long-term outcomes
• Reduces patient loss to follow-up
• Facilitates label expansion studies
• Builds external control arms
• Demonstrates economic value
• Uses tokenization to securely connect datasets
• Integrates into clinical trial workflows with minimal burden to sites and patients

Id

SW1779

Integration Partners

• Medrio EDC
• Veeva Vault
• Clinion EDC
• Castor EDC
• Oracle Clinical

Integrations

• Medidata Rave EDC
• Medidata Health Record Connect
• Medidata eConsent

Languages Supported

• English
• Spanish
• French
• German
• Italian
• Portuguese
• Dutch
• Russian
• Chinese (Simplified)
• Chinese (Traditional)
• Japanese
• Korean
• Arabic
• Hindi
• Bengali
• Punjabi
• Gujarati
• Tamil
• Telugu
• Marathi

Last Updated

2025-10-11

License

Commercial

Market Segment

• Enterprise
• SMB

Optional Modules

Os Platforms

• Web

Pricing Details

Contact vendor for pricing information.

Pricing Model

Subscription

Privacy Features

• BAA available
• Consent management
• Anonymization
• Data minimization

Product Code

SW1779

Product Name

Medidata Link

Ratings

• 4.3 out of 5 stars on Capterra
• 4.4 out of 5 stars on G2
• 4.6 out of 5 stars on G2
• 4.2 out of 5 stars on G2

Regions Available

• United States
• Canada
• European Union
• United Kingdom
• Australia
• Japan
• China
• India
• Brazil
• South Korea
• Mexico
• South Africa
• Russia
• Switzerland
• Singapore
• United Arab Emirates
• Saudi Arabia
• Argentina
• Chile
• Colombia
• Peru

Related Urls

• https://elion.health/products/medidata-link

Release Year

2015

Security Features

• Encryption
• RBAC
• SSO/SAML
• Audit logs
• 2FA
• DLP

Specialties

• Clinical Trials
• Real-world Evidence
• Data Integration
• Patient Data Tokenization
• Clinical Data Management
• Regulatory Compliance
• Data Privacy
• Long-term Follow-up Studies
• External Control Arms
• Label Expansion Studies
• Patient Recruitment
• Data Privacy Certifications
• Clinical Decision Support
• Evidence Generation
• Clinical Data Analytics
• Clinical Trial Optimization
• Patient Engagement
• Site Management
• Clinical Trial Design
• Clinical Trial Execution

Support Channels

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

System Requirements

Target Users

• Clinical Researchers
• Data Scientists
• Clinical Trial Managers
• Regulatory Affairs Professionals
• Biostatisticians
• Pharmaceutical Companies
• Biotech Companies
• Medical Device Manufacturers
• Academic Researchers
• Contract Research Organizations (CROs)

Training Options

• documentation
• webinars
• live_online
• onsite
• certification

Type

product

User Reviews

Version

1.0

Alternatives

See related products

Canonical JSON

{
  "product_name": "Medidata Link",
  "company_name": "Medidata",
  "product_url": "https://www.medidata.com/en/clinical-trial-products/medidata-ai/real-world-data/link-real-world-and-clinical-trial-data/",
  "company_url": "https://www.medidata.com",
  "related_urls": [
    "https://elion.health/products/medidata-link"
  ],
  "product_code": "SW1779",
  "summary": "Medidata Link is a data integration platform that connects clinical trial data with real-world data at the patient level to enhance evidence generation and patient outcomes.",
  "description": "Medidata Link enables the linkage of patient-level clinical trial data with real-world data (RWD) to provide a comprehensive view of the patient journey before, during, and after clinical trials. This integration supports long-term follow-up, reduces patient loss to follow-up, and facilitates the creation of external control arms, thereby accelerating access to innovative treatments while minimizing site burden and costs. The platform is fully integrated with the Medidata Unified Platform and supports various consent models, including paper and eConsent, ensuring seamless data collection across multiple research sites. It also offers pre-built integrations with tokenization technology partners and connects to a broad ecosystem of RWD sources, facilitating secure and compliant data linkage. Medidata Link is designed to be agnostic of consent methods and protects sponsors from the risks associated with directly holding personally identifiable information (PII) by streamlining third-party data privacy certifications. This approach allows sponsors to collect trial data and connect it to patients' RWD, bridging evidence gaps and enhancing confidence in clinical decision-making. The solution is part of Medidata's broader suite of clinical trial products, which aim to optimize clinical trial design, planning, and execution through AI-powered analytics and seamless integration.",
  "categories": [
    "clinical Data Management",
    "data Platform",
    "data Privacy",
    "Clinical Data Management",
    "Health Data Platforms",
    "Patient Data Tokenization"
  ],
  "market_segment": [
    "Enterprise",
    "SMB"
  ],
  "target_users": [
    "Clinical Researchers",
    "Data Scientists",
    "Clinical Trial Managers",
    "Regulatory Affairs Professionals",
    "Biostatisticians",
    "Pharmaceutical Companies",
    "Biotech Companies",
    "Medical Device Manufacturers",
    "Academic Researchers",
    "Contract Research Organizations (CROs)"
  ],
  "specialties": [
    "Clinical Trials",
    "Real-world Evidence",
    "Data Integration",
    "Patient Data Tokenization",
    "Clinical Data Management",
    "Regulatory Compliance",
    "Data Privacy",
    "Long-term Follow-up Studies",
    "External Control Arms",
    "Label Expansion Studies",
    "Patient Recruitment",
    "Data Privacy Certifications",
    "Clinical Decision Support",
    "Evidence Generation",
    "Clinical Data Analytics",
    "Clinical Trial Optimization",
    "Patient Engagement",
    "Site Management",
    "Clinical Trial Design",
    "Clinical Trial Execution"
  ],
  "regions_available": [
    "United States",
    "Canada",
    "European Union",
    "United Kingdom",
    "Australia",
    "Japan",
    "China",
    "India",
    "Brazil",
    "South Korea",
    "Mexico",
    "South Africa",
    "Russia",
    "Switzerland",
    "Singapore",
    "United Arab Emirates",
    "Saudi Arabia",
    "Argentina",
    "Chile",
    "Colombia",
    "Peru"
  ],
  "languages_supported": [
    "English",
    "Spanish",
    "French",
    "German",
    "Italian",
    "Portuguese",
    "Dutch",
    "Russian",
    "Chinese (Simplified)",
    "Chinese (Traditional)",
    "Japanese",
    "Korean",
    "Arabic",
    "Hindi",
    "Bengali",
    "Punjabi",
    "Gujarati",
    "Tamil",
    "Telugu",
    "Marathi"
  ],
  "pricing_model": "Subscription",
  "pricing_details": "Contact vendor for pricing information.",
  "license": "Commercial",
  "company_offices": [
    "United States",
    "France",
    "United Kingdom",
    "Germany",
    "Japan",
    "China",
    "India",
    "Brazil",
    "Australia",
    "Singapore"
  ],
  "company_founding": "1999",
  "deployment_model": [
    "SaaS"
  ],
  "os_platforms": [
    "Web"
  ],
  "features": [
    "Connects patient-level clinical trial data with real-world data (RWD)",
    "Enables longitudinal patient tracking before, during, and after clinical trials",
    "Supports monitoring long-term outcomes",
    "Reduces patient loss to follow-up",
    "Facilitates label expansion studies",
    "Builds external control arms",
    "Demonstrates economic value",
    "Uses tokenization to securely connect datasets",
    "Integrates into clinical trial workflows with minimal burden to sites and patients"
  ],
  "optional_modules": [],
  "integrations": [
    "Medidata Rave EDC",
    "Medidata Health Record Connect",
    "Medidata eConsent"
  ],
  "data_standards": [
    "FHIR",
    "HL7 v2",
    "DICOM",
    "SNOMED",
    "ICD-10"
  ],
  "api_available": "yes",
  "system_requirements": "",
  "compliance": [
    "HIPAA",
    "GDPR",
    "HITECH",
    "SOC 2",
    "ISO 27001",
    "ISO 27017",
    "ISO 27018",
    "ISO 27701"
  ],
  "certifications": [
    "FDA 510(k)",
    "CE/MDR",
    "ONC",
    "ISO 27001",
    "ISO 27017",
    "ISO 27018",
    "ISO 27701"
  ],
  "security_features": [
    "Encryption",
    "RBAC",
    "SSO/SAML",
    "Audit logs",
    "2FA",
    "DLP"
  ],
  "privacy_features": [
    "BAA available",
    "Consent management",
    "Anonymization",
    "Data minimization"
  ],
  "data_residency": "US/EU regions",
  "customers": [],
  "user_reviews": [],
  "ratings": [
    "4.3 out of 5 stars on Capterra",
    "4.4 out of 5 stars on G2",
    "4.6 out of 5 stars on G2",
    "4.2 out of 5 stars on G2"
  ],
  "support_channels": [
    "email",
    "phone",
    "chat",
    "ticketing",
    "community",
    "24x7"
  ],
  "training_options": [
    "documentation",
    "webinars",
    "live_online",
    "onsite",
    "certification"
  ],
  "release_year": "2015",
  "integration_partners": [
    "Medrio EDC",
    "Veeva Vault",
    "Clinion EDC",
    "Castor EDC",
    "Oracle Clinical"
  ],
  "id": "SW1779",
  "slug": "medidata-link",
  "type": "product",
  "version": "1.0",
  "last_updated": "2025-10-11",
  "links_json": {
    "self": "https://www.healthaidb.com/software/medidata-link.json"
  }
}