Will Vytorin Fallout Include ENHANCEd Reporting Requirements For All Trials?
• By Lauren Smith
Companies in heavily regulated industries such as pharmaceuticals often describe congressional investigations under the category of "headline risks": They produce a lot of bad press and a lot of work for the legal, public relations and lobbying arms, but their impact on the core functions of developing and selling drugs is limited
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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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The Center for Biologics Evaluation and Research saw departures far outnumber new hires in the second and third quarters of FY 2025, before more than 100 people left July 14 after the reduction-in-force was finalized.