From cell line development to cGMP DS manufacturing and aseptic filling, the facility is expected to provide end-to-end services for biologics microbial and mammalian-based biologics.
Currently, the new site has fully established process, analytical method development and quality control labs supporting local and international customer projects since summer 2020. The cGMP biomanufacturing suite will contain 500 L microbial and 2,000 L mammalian bioreactors which will be operational in the fourth quarter, representing a capital investment program worth $40 million.
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