In late September, Celltrion received a positive opinion from the European Medicines Agency’s Committee for Medicinal Products for Human Use for its subcutaneous version of biosimilar infliximab, Remsima. (Also see "Celltrion Will Market Subcutaneous Remsima Directly After EU Nod " - Generics Bulletin, 24 September, 2019.)
In this podcast, David Wallace, executive editor of Generics Bulletin, talks to Duncan Emerton, biosimilars expert and director at Informa Pharma Consulting, about
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