ArticleHealth affairs scholar2026
Prevalence of ties to industry-funded organizations among patient and consumer representatives on FDA advisory committees.
Article in Health affairs scholar, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: FDA advisory committees are primarily composed of scientific experts, but also include a patient representative and a consumer representative providing public perspectives. Although the FDA has enacted policies to curb conflicts of interest common among its scientific members, it has paid less attention to potential conflicts arising from patient and consumer representatives who have ties to organizations financially supported by pharmaceutical companies. Methods: We analyzed the prevalence of industry funding of advocacy organizations in which patient and consumer representatives were actively involved in the year they attended FDA advisory committee meetings between 2013 and 2022. Results: Between 2013 and 2022, nearly 2 in 5 (38%) FDA advisory committee meetings included either a patient or consumer representative with active ties to a pharmaceutical-funded advocacy organization. For several FDA committees, this share was greater than 50%. More than 1 in 10 (11%) advisory committee meetings included a representative affiliated with an organization receiving funds from the sponsor of the drug under review. Conclusion: These prevalence rates show that these organizational relationships extend beyond isolated cases and signal a broader problem warranting FDA policy attention.
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