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On June 2, Celltrion announced that they will embark on the approval procedure of biosimilar 'Remsima' in the United States.
According to Celltrion, they plan to submit permission application for sales in the U.S. based on the result of global phase 1, 3 clinical trial and result of clinical trial conducted in the U.S. If they submit permission application, it is expected to take about 1 year ...