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2022
MayAdded 4×2000L single-use bioreactors. 13,000L total GMP drug substance capacity
MarPassed Third party US FDA Audit
JanAseptic filling capacity expanded to 15 million units per annum: vials, cartridges and prefilled syringes
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2021
DecDelivered 2,000 L clinical phase 2 product
MayDoubled GMP Drug Substance purification capacity
JanExpanded GMP Drug Substance to 2000L scale
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2020
NovPassed QP Audit; Received NMPA《Drug Manufacturing License》
JunGMP Drug Substance line started operation to 500L
JanQC Laboratories completed
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2019
DecPD/AD laboratories ready
Kilo lab for preclinical lots to scale of 250L readyJulNew facility move-in; First 2 projects kicked off
AprBioworkshops registered
