Talu ai nei, na maua ai e le JYMed's peptide production facility, Hubei Jianxiang Biopharmaceutical Co., Ltd., ni pepa aloaia se lua na tuʻuina atu e le Hubei Provincial Drug Administration: o le "Drug GMP Compliance Inspection Result Notification" (No. E GMP 2024-258 ma Nu. E GMP 2024-260) ma le EU Pharmaceutical Ingredients 2024-260. (API) Tusi Faamaonia” (WC Certificate, Nu. HB240039).
O nei pepa faʻamaonia e faʻamaonia ai o le laina gaosiga A102 i le Workshop A102 (mo le gaosiga o Oxytocin ma Semaglutide APIs) ma le laina gaosiga A092 i le Workshop A092 (mo le gaosiga o Terlipressin API) i Hubei Jianxiang e faʻafetaui tulaga GMP a Saina, lea e tutusa ma le EU, World Health Organization (WHOMP), ma le ICH7 Organisation for Health Organization (WHOMP).
Na fa'ai'u le asiasiga i le tausisia, e fa'ailoa mai ai o le fa'atonuga lelei o le gaosiga ma faiga fa'atonutonu a le Hubei Jianxiang e fetaui ma tulaga maualuga i totonu o le atunu'u. O lenei atinaʻe o le a lagolagoina ai le faʻalauteleina o Hubei Jianxiang i le maketi o le lalolagi, aemaise lava i le maketi a le EU, faʻaleleia le faʻatuatuaina o tagata faʻatau, faʻaleleia fegalegaleaiga faʻavaomalo, ma saofagā i le tuputupu aʻe o le lalolagi ma tufatufaina atu o vailaʻau faʻavae peptide. Aʻo faʻateleina manaoga maketi faavaomalo, Hubei Jianxiang o le a sili atu ona faʻatulagaina e faʻafetaui manaʻoga o tagata faʻatau i le lalolagi ma oloa ma auaunaga maualuga.
E uiga i le JYMed
Faʻavae i le 2009, Shenzhen JYMed Technology Co., Ltd. o se kamupani biotechnology faʻapitoa i suʻesuʻega tutoʻatasi, atinaʻe, gaosiga, ma le faʻatau atu o oloa peptide, faʻatasi ai ma aganuʻu peptide R&D ma auaunaga gaosiga. O loʻo ofoina atu e le kamupani le 20 peptide API, faʻatasi ai ma oloa e lima, e aofia ai Semaglutide ma Tirzepatide, ua maeʻa faʻamaeʻaina faʻamaumauga a le US FDA DMF.
O le Hubei JX fale o lo'o fa'aalia 10 laina gaosiga mo peptide APIs (e aofia ai laina pailate-scale) e ogatasi ma tulaga cGMP a le US, EU, ma Saina. O lo'o fa'agaoioia e le fale se fa'atonuga lelei o vaila'au fa'apitoa ma le EHS (Si'osi'omaga, Soifua Maloloina, ma le Saogalemu). Ua pasia e le NMPA su'esu'ega a le GMP ma su'ega a le EHS na fa'atautaia e tagata fa'atau i le lalolagi.
Au'aunaga Autu
- Resitala API peptide i totonu o le atunuu ma faavaomalo
- peptides fa'afoma'i ma cosmetic
- Fa'asologa peptide fa'apitoa, CRO, CMO, ma auaunaga OEM
- PDC (Peptide Drug Conjugates), e aofia ai peptide-radionuclide, peptide-laiti mole, peptide-protein, ma peptide-RNA conjugates
Fa'amatalaga Fa'afeso'ota'i
tuatusi:8th & 9th Floors, Fale 1, Shenzhen Biomedical Innovation Industrial Park, Jin Hui Road 14, Kengzi Street, Pingshan District, Shenzhen, Saina
Mo Su'esu'ega API Fa'avaomalo:
+86-755-26612112 | +86-15013529272
Mo Mea Fa'aigoa Peptide Matagofie ile Fale:
+86-755-26612112 | +86-15013529272
Mo le Resitala API ile Aiga ma Auaunaga CDMO:
+86-15818682250
Upega tafa'ilagi: www.jymedtech.com
Taimi meli: Ian-10-2025







