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Following GenScript Biotech Corporation's cPass™ SARS-CoV-2 Neutralization Antibody Detection Kit has received provisional authorization by Health Science Authority (HSA) Singapore on 8th May 2020, CE-IVD marking in Europe on 26th May 2020 and FDA ...
GenScript Biotech announced the company has filed for Emergency Use Authorization (EUA) with the U.S. Food and Drug Administration (FDA) to market its cPass™ SARS-CoV-2 Neutralization Antibody Detection Kit.
Biologics commercial production centre will be the first and largest such facility in China covering cell therapy, gene therapy and antibody-drug R&D to meet the production needs of pre-clinical and phase I clinical samples