Trusted Research Environment
Secure analysis where the data lives
Trusted Data Lakehouse
Connect and catalog distributed data
Federation
Query many sites as one, nothing moves
TrustOps & Airlock
Keeps data in place, secured with Airlock controls
AI Scientist Studio
AI Scientists that work inside your TRE
Sovereign AI
Run models where the data lives
Trusted DataHub
Query federated data instantly
Lifebit R.E.A.L.
Real-time drug safety surveillance
Trusted Data Factory
OMOP and FHIR harmonization at scale
Trusted TargetID
Validate drug targets on real cohorts
Rapid Data Products
Curated datasets, delivered fast
Trusted Data Marketplace
Discover data on 275M+ patients
New
AI Scientists that run inside your Trusted Research Environment. Data never leaves the source.
See the Studio →
All products →
Pricing & plans →
Trust Center →
Government
National health data programs
Commercial pharma
Discovery, trials and real-world evidence
Health systems
Clinical data for research and care
Health nonprofits
Cohorts and registries, safely shared
Biobanks & data providers
Make data usable without releasing it
Target validation
Clinical trial optimization
Patient registries
ADR & outbreak surveillance
Population genomics
Data harmonization (OMOP, FHIR)
NGS data analysis
Customer story
“I am incredibly excited that Lifebit joined us to launch the next phase of our research capabilities.” Chris Wigley, former CEO
Read the case study →
All use cases →
All customer stories →
Blog
White papers
Publications
Customer stories
News
About us
Careers
Technology partners
Trust Center
Contact us
Help center
Book a demo
Pricing & plans
Latest white paper
How pharma teams use federated real-world data without moving a record.
Read the white paper →
Federated TRE guide →
What is a TRE? →
Home/Blog/Maria Chatzou Dunford
The Library
Newest first.
Searching…
Search is not available right now.
All830Trusted Research Environment71Technology469Industry215Announcements69Opinion26
413 articles · page 8 of 35
Managing clinical trial data effectively is critical for regulatory compliance and faster drug approvals. This comprehensive guide evaluates the 9…
Clinical research organizations handling sensitive patient data face unprecedented security challenges as cyberattacks surge and regulatory scrutiny…
Clinical genomics workflow platforms bridge the critical gap between generating sequencing data and delivering actionable clinical insights while…
A clinical data standardization platform transforms incompatible health records from multiple sources—hospitals using different EHR systems…
Biotech organizations struggle with fragmented research data scattered across silos while navigating strict compliance requirements like HIPAA and…
Biopharma R&D teams waste months merging incompatible clinical, genomic, and real-world datasets due to conflicting standards and regulatory…
This step-by-step guide shows R&D leaders how to unify genomic data, clinical records, and real-world evidence into a single queryable environment.…
Managing biobank data across institutions requires systems that harmonize genomic, clinical, and consent data while maintaining regulatory…
Choosing the best secure research environment platforms requires evaluating compliance certifications like FedRAMP, HIPAA, and GDPR alongside…
Biopharma R&D teams struggle with siloed genomic, clinical, and regulatory data across multiple formats and compliance frameworks. This comprehensive…
Automated clinical data curation uses AI to transform incompatible clinical data from multiple sources into standardized, research-ready datasets in…
AI powered drug target discovery is transforming pharmaceutical development by using machine learning to analyze fragmented biological…
