The PhRMA annual meeting took place just days before the make or break vote on health care reform. Here is a sampling of what speakers at that event said about how industry should feel about the legislation.
"Historic" is a word used frequently in the context of health care reform, but living in the uncertainty of history-making legislation isn't quite the same thing.
Among the many unbelievable elements of the twists and turns in the reform debate was the timing of the Pharmaceutical...
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.’
While treatments for scleroderma are in development, none are approved for the condition that is associated with high morbidity and mortality. The European Medicines Agency says guidance on how to design development programs for the disorder is needed.
Madrigal Pharmaceuticals’ Rezdiffra is on track to become the first medicine approved in the EU for non-cirrhotic metabolic dysfunction-associated steatohepatitis after the European Medicines Agency recommended that it be granted conditional marketing authorization.
Highlights from Day Four of the BIO International Convention include policy concerns helping constrain dealmaking, Novartis discussing its approach to partnering, and Generate looking for funding to move into Phase III.
