FDA's modernization efforts are essential for the agency to succeed as a regulatory organization in the future, but there will be no "quick fix," FDA Commissioner Andrew von Eschenbach said March 26 in an address to the Food and Drug Law Institute's annual conference
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Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.
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A new pilot aims to take Brazil closer to ‘digital transformation.’
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The transparency initiative collects CRLs already made public in approval packages on its drugs@fda site to post on the openFDA public portal.
FDA staff are trying to plan for program implementation in the absence of critical eligibility and other details, although guidance may be coming soon.
