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The FDAs response assessment: corrective actions found deficient The firm submitted two responses to the Form FDA 483 and initiated a voluntary recall of all drug products within expiry that had OOS results
Our conclusions would also be strengthened by repeating our analysis with a control group, comparing patients who switched to semaglutide with those who remained on their index GLP-1 RA or who switched to a different GLP-1 RA, such as dulaglutide
Benoist CC, Wright JW, Zhu M, Appleyard SM, Wayman GA, Harding JW
26 , 198211.e5 (2017)
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