Congenica platform

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

Company Name

Congenica

Product URL

https://www.congenica.com

Company URL

https://www.congenica.com

Categories

• clinical Decision Support
• genomics
• precision Medicine
• diagnostic Support
• health Data Analytics
• Genomic Analysis
• Diagnostic
• Clinical Informatics

Summary

Congenica offers a genomic analysis platform that enables rapid interpretation of complex genomic data to support precision medicine and improve patient outcomes.

Description

Congenica provides a scalable, automated platform for analyzing and interpreting genomic data, supporting areas such as inherited diseases, somatic cancer, pharmacogenomics, and pathogen surveillance. The platform is CE-IVD approved and integrates with existing healthcare systems to streamline clinical workflows.

Api Available

yes

Certifications

• CE Marked IVD under In Vitro Diagnostics Directive (98/79/EC)
• ISO 27001
• ISO 13485
• ISO 14971
• ISO 62304
• ISO 82304
• ISO 62366
• ISO 28000:2007
• Cyber Essentials Plus
• NHS Digital Data Security and Protection Toolkit
• NHS Information Governance Toolkit (IGT)

Company Founding

2014

Company Offices

• United Kingdom
• United States
• China

Compliance

• HIPAA
• GDPR
• ISO 27001
• ISO 13485
• ISO 14971
• ISO 62304
• ISO 82304
• ISO 62366
• ISO 28000:2007
• Cyber Essentials Plus
• NHS Digital Data Security and Protection Toolkit
• NHS Information Governance Toolkit (IGT)

Customers

• National Health Service (NHS) Genomic Medicine Service
• SeqOne
• Wellcome Sanger Institute
• UK NHS
• Leading international laboratories
• Academic medical centres
• Hospitals
• Biopharmaceutical companies

Data Residency

EU-only

Data Standards

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

Deployment Model

• SaaS
• on_prem
• hybrid

Features

• Automated genomic data analysis
• Clinical decision support
• Variant pathogenicity predictions
• Integration with existing medical records
• Integration with laboratory management systems
• Flexible deployment options
• Rapid analysis and interpretation of next-generation sequencing data
• Scalable platform for large-scale genomic data analysis
• Support for inherited diseases
• Support for somatic cancers
• Support for pathogen surveillance
• Support for prenatal health
• Support for carrier screening
• Support for neurodevelopmental disorders
• Support for solid tumors
• Support for rare diseases
• Support for inherited cancers
• Support for pharmacogenomics

Id

SW2768

Integration Partners

• SeqOne
• Wellcome Sanger Institute
• UK NHS
• Leading international laboratories
• Academic medical centres
• Hospitals
• Biopharmaceutical companies

Integrations

• Electronic Health Records (EHRs)
• Laboratory Information Management Systems (LIMS)

Languages Supported

• English

Last Updated

2025-10-11

License

commercial

Market Segment

• enterprise
• smb
• consumer

Optional Modules

• Clinical Interpretation Services
• Professional Services
• Customer Support
• Pharma Services

Os Platforms

• Web
• iOS
• Android
• Windows
• macOS
• Linux

Pricing Details

Contact vendor for pricing information.

Pricing Model

subscription

Privacy Features

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

Product Code

SW2768

Product Name

Congenica platform

Ratings

• CE-IVD approved software

Regions Available

• United Kingdom
• European Union
• United States
• China
• Iceland
• Liechtenstein
• Norway
• Switzerland
• Turkey

Related Urls

Release Year

2014

Security Features

• Data encryption
• Role-based access control (RBAC)
• Single sign-on (SSO)
• Audit logs
• Two-factor authentication (2FA)
• Data loss prevention (DLP)

Specialties

• Rare Diseases
• Inherited Cancers
• Neurodevelopmental Disorders
• Prenatal Health
• Somatic Oncology
• Pathogen Surveillance
• Pharmacogenomics

Support Channels

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

System Requirements

• Windows Server
• Linux Server
• macOS Server

Target Users

• clinicians
• geneticists
• laboratory technicians
• healthcare administrators
• researchers

Training Options

• documentation
• webinars
• live_online
• onsite
• certification

Type

product

User Reviews

• The platform's automation significantly reduces the burden on specialist staff, enhancing case throughput and accelerating decision-making.
• CE-IVD approved software ensures accurate and secure analysis, supporting clinical decisions with high confidence.
• Offers ultimate flexibility, accommodating various needs from gene panels to whole genomes, both SaaS and on-premise.
• Easy-to-integrate solution with APIs compatible with existing workflow solutions, LIMS systems, and EHRs, optimizing operational efficiency.

Version

1.0

Alternatives

See related products

Canonical JSON

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  "company_name": "Congenica",
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  "company_url": "https://www.congenica.com",
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  "product_code": "SW2768",
  "summary": "Congenica offers a genomic analysis platform that enables rapid interpretation of complex genomic data to support precision medicine and improve patient outcomes.",
  "description": "Congenica provides a scalable, automated platform for analyzing and interpreting genomic data, supporting areas such as inherited diseases, somatic cancer, pharmacogenomics, and pathogen surveillance. The platform is CE-IVD approved and integrates with existing healthcare systems to streamline clinical workflows.",
  "categories": [
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  "company_founding": "2014",
  "deployment_model": [
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    "hybrid"
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  "os_platforms": [
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  "features": [
    "Automated genomic data analysis",
    "Clinical decision support",
    "Variant pathogenicity predictions",
    "Integration with existing medical records",
    "Integration with laboratory management systems",
    "Flexible deployment options",
    "Rapid analysis and interpretation of next-generation sequencing data",
    "Scalable platform for large-scale genomic data analysis",
    "Support for inherited diseases",
    "Support for somatic cancers",
    "Support for pathogen surveillance",
    "Support for prenatal health",
    "Support for carrier screening",
    "Support for neurodevelopmental disorders",
    "Support for solid tumors",
    "Support for rare diseases",
    "Support for inherited cancers",
    "Support for pharmacogenomics"
  ],
  "optional_modules": [
    "Clinical Interpretation Services",
    "Professional Services",
    "Customer Support",
    "Pharma Services"
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  "integrations": [
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    "Laboratory Information Management Systems (LIMS)"
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  "data_standards": [
    "FHIR",
    "HL7 v2",
    "DICOM",
    "SNOMED",
    "ICD-10"
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  "api_available": "yes",
  "system_requirements": [
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    "Linux Server",
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  ],
  "compliance": [
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    "GDPR",
    "ISO 27001",
    "ISO 13485",
    "ISO 14971",
    "ISO 62304",
    "ISO 82304",
    "ISO 62366",
    "ISO 28000:2007",
    "Cyber Essentials Plus",
    "NHS Digital Data Security and Protection Toolkit",
    "NHS Information Governance Toolkit (IGT)"
  ],
  "certifications": [
    "CE Marked IVD under In Vitro Diagnostics Directive (98/79/EC)",
    "ISO 27001",
    "ISO 13485",
    "ISO 14971",
    "ISO 62304",
    "ISO 82304",
    "ISO 62366",
    "ISO 28000:2007",
    "Cyber Essentials Plus",
    "NHS Digital Data Security and Protection Toolkit",
    "NHS Information Governance Toolkit (IGT)"
  ],
  "security_features": [
    "Data encryption",
    "Role-based access control (RBAC)",
    "Single sign-on (SSO)",
    "Audit logs",
    "Two-factor authentication (2FA)",
    "Data loss prevention (DLP)"
  ],
  "privacy_features": [
    "Business Associate Agreement (BAA) available",
    "Consent management",
    "Anonymization",
    "Data minimization"
  ],
  "data_residency": "EU-only",
  "customers": [
    "National Health Service (NHS) Genomic Medicine Service",
    "SeqOne",
    "Wellcome Sanger Institute",
    "UK NHS",
    "Leading international laboratories",
    "Academic medical centres",
    "Hospitals",
    "Biopharmaceutical companies"
  ],
  "user_reviews": [
    "The platform's automation significantly reduces the burden on specialist staff, enhancing case throughput and accelerating decision-making.",
    "CE-IVD approved software ensures accurate and secure analysis, supporting clinical decisions with high confidence.",
    "Offers ultimate flexibility, accommodating various needs from gene panels to whole genomes, both SaaS and on-premise.",
    "Easy-to-integrate solution with APIs compatible with existing workflow solutions, LIMS systems, and EHRs, optimizing operational efficiency."
  ],
  "ratings": [
    "CE-IVD approved software"
  ],
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  "integration_partners": [
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    "Academic medical centres",
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    "Biopharmaceutical companies"
  ],
  "id": "SW2768",
  "slug": "congenica-platform",
  "type": "product",
  "version": "1.0",
  "last_updated": "2025-10-11",
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    "self": "https://www.healthaidb.com/software/congenica-platform.json"
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}