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Hybio Pharmaceutical Liraglutide jekiseni rakabvumidzwa neUS FDA

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Hybio Pharmaceutical Liraglutide jekiseni rakabvumidzwa neUS FDA

2024-07-17

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2021.09——IWE Kutumira kwokutanga

2021.10——ANDA yakagamuchirwa zvakabudirira

2021.11——Liraglutide raw material yakanyoreswa neDMF

2023.10——Hybio Pharmaceuticals 'subsidiary, (hwaro hwekugadzirwa kwegadziriro) Bazi rePingshan, rakapedza ongororo yakaitwa neUnited States Food and Drug Administration (FDA) yezvazvino Good Manufacturing Practices (cGMP)

2023.11——Hybio Pharmaceuticals’subsidiary, (nheyo yeRaw material pharmaceutical) WuHan Branch, yakapedza ongororo yepanzvimbo neUnited States Food and Drug Administration (FDA) yezvino Good Manufacturing Practices (cGMP)

2023.12——Kambani yevabereki veHybio Pharmaceuticals, (yepakati peKutsvagisa nebudiriro) yakapedza kuongororwa pasaiti neUnited States Food and Drug Administration (FDA) yezvazvino Good Manufacturing Practices (cGMP)

2024.02——NFC mhinduro dzawanikwa dze liraglutide

2024.03—— Pedzisa kutenderera kwekupedzisira kweCRL mhinduro

2024.06--Batch rekutanga rejekiseni reLiraglutide rakaendeswa kuUnited States uye rakapedzisira ragamuchira mvumo kubva kuUS FDA.