Amarin Seeks AMR101 Approval; Hopes To Begin Commercialization Of First Product
The New Jersey biotech submitted the NDA for its omega-3 fatty acid drug with FDA.
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Newly introduced rules for streamlining drug registration in Vietnam are said to present both opportunities and challenges for stakeholders.
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At Medicines for Europe’s legal and annual conferences in Brussels last week, multiple key issues competed for attention, giving the generics and biosimilars industry plenty to think about at a critical time for EU pharma reform.
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The creation of a single national formulary for medicines prescribing that could impact industry is among the action points in the UK government’s new 10-year health plan for the National Health Service in England.