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Last year, we noted a new trend in warning letter language specifically concerning teleconferences between FDA and a firm regarding the initiation of a voluntary recall

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Following a review completed in 2024, the EMA's Pharmacovigilance Risk Assessment Committee (PRAC) concluded that available evidence did not support a causal link between GLP-1 receptor agonists and suicidal ideation or self-harm, a conclusion also reflected in MHRA communications that year