The National Institutes of Health's Office of Dietary Supplements and the National Library of Medicine are investigating the development of a user-friendly online catalogue of labels for dietary supplement sold in the U.S. If viable, the database will build on the current Dietary Supplement Label Database, ODS says in an Aug. 1 release. Federal and stakeholder user groups will determine the content of the database, which will be an "important information resource on the ingredients in dietary supplements"...
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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.’
The EU product information for Novo Nordisk’s semaglutide medicines is to be updated to include non-arteritic anterior ischemic optic neuropathy as a side effect with a frequency of “very rare.”
The Pink Sheet explores how regulatory approvals for Leqembi differ around the world, and looks at what is coming next.
Experts from EUCOPE explain why the Council of the EU’s position on the proposed overhaul of the general pharmaceutical legislation could offer more predictability for companies than the commission’s initial offering.
