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Clinical data show that MHRA received 7,228 reports of gastrointestinal reactions with GLP-1 receptor agonists, whilst independent testing of unregulated peptides revealed significant purity discrepancies, with some products showing purity levels as low as 1.7% compared to supplier claims

Comment: One commenter opined that all of the nominated devices included in the CY2026 OPPS/ASC proposed rule meet the criteria for device pass-through

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