Dingell Says Lab Closures “Frightening,” FDA District Chief Expects Problems
House Energy and Commerce leaders say FDA's plan to close several labs - including its only facility testing for radiological contaminants - is a threat to national security, while an FDA district chief says problems are likely to hinder the agency's work early in the planned reorganization
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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.’
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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Blenrep, GSK’s multiple myeloma therapy, faced a major setback when it was withdrawn from the market in 2022.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.