PRIVATE-LABEL LOPERAMIDE ENCROACHING ON OTC ANTIDIARRHEAL MARKET, accounting for the majority of the 8.7% share of the market held by private-label antidiarrheals during the 12 months through February 1994, according to Information Resources, Inc. subsidiary Towne-Oller & Associates. The 8.7% share represents an increase of more than 6 share points from the 2% market share held by private-label antidiarrheals in the previous 12-month period.
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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.’
Too many “uninformative” drug trials fail to justify the excessively high prices of many medicines, while there is too much evidentiary uncertainty in European pricing and reimbursement systems, warned Anja Schiel from Norway’s NOMA.
It appears that the European Medicines Agency is making progress on its re-examination of Eli Lilly’s Alzheimer’s disease drug Kisunla, following an initial rejection in March based on safety concerns.
Health Canada’s proposal to no longer require biosimilar manufacturers to prove the safety and efficacy of their product through Phase III clinical trials marks a pivotal change in Canada’s regulatory approach.
