Schering-Plough recalls four lots of Intron A (interferon alfa-2b) after stability tests find it to be subpotent 30 days following reconstitution. The lots are manufactured at company's Ireland plant; Schering is sorting out cGMP compliance problems at its Puerto Rico and New Jersey facilities (1"The Pink Sheet" July 2, p. 25). The recalled lots were due to expire between Oct. 20 and Aug. 2, 2002
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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.’
Recent and upcoming US FDA advisory committee meetings and a summary of the topics covered.
The UK’s research-based pharma industry and medical research charities have set out clear action points to drive greater diversity and inclusion in clinical trials.
Blenrep, GSK’s multiple myeloma therapy, faced a major setback when it was withdrawn from the market in 2022. The drug has since made a return as a second-line therapy, and is on track to being reimbursed in England.
