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Furthermore, regulatory approval requires case-by-case evaluation by authorities such as the FDA and European Medicines Agency, emphasising the need for manufacturing consistency and comprehensive safety evaluations [178]

doi: 10.1007/s10571-023-01365-1 353 SunX.-Y.WeiY.-P.XiongY.WangX.-C.XieA.-J.WangX.-L.et al

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[accessed 08 Jul 19] Health Service Executive (HSE) (2019) Healthcare audit [quality assurance and verification]

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