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GMP Production Suite scales up capacity for preclinical, clinical and early launch needs for proprietary and partnered programs
December 3, 2019
By: Kristin Brooks
Managing Editor, Contract Pharma
CureVac AG, a clinical stage biopharmaceutical company in the field of mRNA-based drugs, received manufacturing authorization for clinical trial materials produced under Good Manufacturing Practice (GMP) from the Regierungspräsidium Tübingen (as representative of the European Medicines Agency), for the company’s scaled up GMP III production suite. This license marks CureVac’s third production suite to manufacture at GMP pharmaceutical production. CureVac’s GMP I, II and III production suites are...
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