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The practice of sharing summary results, clinical study reports, individual patient data, and trial registration for prospective and retrospective trials.
Multiple reproducible models exist for sharing patient‑level clinical trial data that balance privacy and commercial confidentiality: technical anonymization standards and privacy metrics, governance ...
and regulator summaries are curated, document-level narratives and aggregated analyses of trials, while individual participant data (IPD) are the raw, participant‑level records that underlie those sum...
The 2017 structured audit of 42 major pharmaceutical companies concluded that corporate were highly variable, and that “other than journal submission for all trials within 12 months, all elements of b...
No provided reporting documents a pharmaceutical company releasing the complete raw, patient‑level data for a major statin trial; existing sources describe long-standing calls for broader trial data s...