FDA has postponed a joint meeting of FDA's Dermatologic Drugs and Anti-Infective Drugs Advisory Committees, originally scheduled for Sept. 23, to examine the potential for antibiotic resistance if topical erythromycin were to be made available OTC as an acne treatment. In a Sept. 9 Federal Register notice, the agency said it postponed the session to allow more time to find speakers. The meeting is expected to be rescheduled in a few months
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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 European Medicines Agency says that a regulatory reliance pilot that it is supporting to speed up assessments of post-approval changes appears to be accelerating evaluation timelines in non-EU countries.
The UK regulator’s draft guideline on the use of external control arms based on real-world data reflects concepts similar to those outlined by the US Food and Drug Administration.
The Pink Sheet's list of EU centralized approvals of new active substances has been updated to include two new products, one of which is Vyjuvek, Krystal Biotech's advanced therapy for treating dystrophic epidermolysis bullosa.
