Transparency in the existence, use, and output of a mental health data resource: a descriptive paper from the National Institute for Health and Care Research (NIHR) Maudsley Biomedical Research Centre (BRC) Clinical Record Interactive Search (CRIS) Platform

Minimum elements for reporting a feasibility assessment of algorithms based on routinely collected health data for multi-jurisdiction use: Health Data Research Network Canada recommendations

Integrating public engagement to promote transparent data use in a new UK-wide birth cohort

Extent of Open Science Practices in the Reporting of Real World Evidence Research

Improving transparency in data access processes: Developing best practice standards and promoting system-wide change through a competitive funding call

Semi-automated data provenance tracking for transparent data production and linkage to enhance auditing and quality assurance in Trusted Research Environments

Characterising firearm-related databases across Canada: opportunities for data linkage to inform understanding of injury burden and prevention

Open science and phenotyping in UK administrative health, education and social care data: the ECHILD phenotype code list repository

Co-developing resources for better public understanding of Longitudinal Population Study Data and the Law

Data Dictionaries: Essential Tools for the Ethical and Transparent Use of Integrated Data

A Review of Synthetic Data Terminology for Privacy Preserving Use Cases

Four checks for low-fidelity synthetic data: recommendations for disclosure control and quality evaluation