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Repositories and other initiatives
In this section, we are studying data sharing platforms, repositories and indeed any other initiative.

01
STATUS OF SHARING OF INDIVIDUAL PARTICIPANT DATA FROM CLINICAL TRIALS, USE OF SHARED DATA AND IMPACT OF RESEARCH OUTPUTS OF SHARING DATA
02
ATTENTION AND IMPACT OF SHARING INDIVIDUAL PARTICIPANT DATA FROM CLINICAL TRIALS: A CROSS SECTIONAL ANALYSIS OF PUBLISHED RE-USE FROM 3 MAJOR REPOSITORIES


03
INFERENTIAL REPRODUCIBILITY OF THERAPEUTIC RESEARCH: A CROSS-SECTIONAL STUDY OF RANDOMIZED CONTROLLED TRIALS AVAILABLE ON MAJOR DATA-SHARING PLATFORMS
This registered report introduces a cross-sectional study aiming to assess inferential reproducibility (qualitatively similar conclusions can be drawn from a reanalysis of the original trials) for main RCTs available on major data-sharing platforms.
Protocol / Work in progress, in principle acceptance at Royal Society Open Science
04
IMPLEMENTING CLINICAL TRIAL DATA SHARING REQUIRES TRAINING A NEW GENERATION OF BIOMEDICAL RESEARCHERS
A policy forum "Implementing clinical trial data sharing requires training a new generation of biomedical researchers" proposes an agenda that aims to train a new generation of experts for clinical trial data sharing.


05
TEN (NOT SO) SIMPLE RULES FOR CLINICAL TRIAL DATA-SHARING
We propose 10 (not so) simple rules for researchers wishing to share data, aligned on the clinical trial lifecycle. These rules cover the majority of elements to be considered in order to start the commendable process of clinical trial data-sharing.
Paper
06
MAKING DATA-SHARING THE NORM IN MEDICAL RESEARCH
In this editorial, we comment on the low data sharing rates observed in the biomedical literature. We discuss the scientific and ethical value of clinical trial data sharing and call various stakeholders to act in order to make clinical trial data sharing a norm for biomedical research.
Paper

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