Dietary Supplement Quality Demonstration Program to be headed by new VP Forouz Ertl, who also will help form Department of Dietary Supplement Quality to be overseen by COO John Fowler, USP announces May 7. Ertl and Fowler will be responsible for implementing QDP, which is in its pilot stage (1"The Tan Sheet" Feb. 26, p. 20). Ertl already has served on USP's Dietary Supplements Botanicals Expert Committee and other USP panels. She previously worked for Zuellig Group North America and Botanicals International
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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.
