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2012

GMP inspection for the facility and new products was completed.
Pharmigene’s HLA-B*5801 Assessment Test received approval from the Department of Health, Taiwan.
A new manufacturing plant was built, and the headquarter relocated to Taipei (Neihu).
ISO / CE IVD 2012 annual inspection was completed.
Pharmigene’s HLA-B*5701/3101 received IVD List B CE certification (Verification Unit: SGS)

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