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 7 of 35
Master public health data analysis in Canada: Access Ontario datasets, track opioids, AMR, & chronic diseases with expert tools & trends.
Navigating genomic data privacy regulations requires balancing research innovation with stringent protection requirements across multiple frameworks…
Genomic data analysis compliance requirements demand a specialized framework that goes beyond traditional healthcare data protection, as genetic…
Building a GDPR compliant research environment requires understanding Article 89's scientific research provisions and implementing specific technical…
A FedRAMP authorized healthcare platform meets stringent federal security standards essential for government health agencies and biopharma companies…
Managing genomic data at enterprise scale requires platforms that handle petabytes of sensitive sequencing data while maintaining compliance and…
A drug discovery data platform solves the critical infrastructure problem slowing pharmaceutical R&D by unifying fragmented data sources—genomics…
Government health agencies and biopharma companies can now conduct cross-border health data analysis without violating GDPR, HIPAA, or sovereignty…
Managing genomic data at scale requires balancing massive storage needs with strict regulatory compliance—a single genome generates 200GB, and…
Healthcare organizations managing sensitive patient data face an impossible choice between research productivity, regulatory compliance, and security…
As genomic sequencing generates petabytes of data that overwhelm on-premise systems, cloud-based genomic analysis platforms have become essential for…
The clinical trial data silos problem occurs when research data becomes fragmented across multiple sites, systems, and repositories, delaying…
