[DOI] [PMC free article] [PubMed] [Google Scholar] 91.Bostrm P., Wu J., Jedrychowski M.P., Korde A., Ye L., Lo J.C., Rasbach K.A., Bostrm E.A., Choi J.H., Long J.Z., et al
Procurement officers should verify the current authorisation status directly against the MHRA medicines register before drafting institutional documentation, because the regulatory position can shift quickly once Phase 3 data is filed
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