The Pulmonary-Allergy Drugs Advisory Committee’s discussion of Novartis’ Arcapta Neohaler on March 8 briefly veered off in a direction that surely no sponsor wants to see, with panelists debating whether a drug should be dosed less frequently for economic reasons than proposed by the sponsor.
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The UK drug regulator and England’s health technology assessment agency have joined forces under an information sharing agreement, aimed at accelerating patient access to newly approved medicines by three to six months.
A newly launched UK government inquiry is seeking to learn how viable it would be to bring back domestic control over the entire drug manufacturing pipeline.
Learn how advances in vaccine adjuvants are shaping the future of global health and driving more effective immunization strategies
