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98 articles · page 6 of 9
Genomic data governance is the system of policies, roles, technical controls, and accountability mechanisms that determines how genomic data is…
Boehringer Ingelheim and Lifebit renew their three-year partnership, deepening use of a secure, federated Trusted Research Environment to accelerate…
Data residency requirements are legal or regulatory rules that determine where health data may be physically stored and processed — typically…
A data clean room is a neutral computing environment — originating in advertising technology — where two or more parties match and analyze their…
Under the General Data Protection Regulation (GDPR), anonymization and pseudonymization are legally distinct concepts with opposite consequences.…
Output checking is the process of reviewing every result a researcher wants to take out of a Trusted Research Environment (TRE) — tables, figures…
A Data Access Committee (DAC) is the governance body that reviews and decides applications from researchers who want to use a sensitive dataset…
Differential privacy is a mathematical framework that limits how much any single individual's data can influence the output of an analysis, by adding…
Synthetic health data is artificially generated data that mimics the statistical properties of real patient data without corresponding to real…
The European Health Data Space (EHDS) is a European Union regulation — Regulation (EU) 2025/327 — that creates a common legal framework for using…
Centralized data governance copies datasets into a single repository, making harmonization easy but creating regulatory, security and scalability…
The Five Safes framework is the canonical model for governing research access to sensitive data, comprising Safe People, Safe Projects, Safe…
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