For decades, the FDA has long been thought of as a steady hand of gold-standard regulatory work for the most innovative drugs in the world.
This year, the agency has looked more like a reality …
In Laura Jensen’s first 90 days at GoodRx, she’s found herself spending quite a lot of time on what’s happening in Washington, DC. Jensen joined
The ESSENCE trial of Sarepta’s Vyondys 53 and Amondys 45 failed to hit its objective, placing their FDA accelerated approvals at risk.
Figuring out how to transport genetic medicines to the right parts of the body remains one of the great technical challenges constraining CRISPR’s potential. Now,
CDMO executives say they are unfazed about the wave of pharma companies boosting their internal manufacturing capacity as they onshore to the US, noting this
CDR-Life has inked a second licensing pact with Boehringer Ingelheim, as the Zurich-based startup will work with the German drug company in a ripe area
For decades, the FDA has long been thought of as a steady hand of gold-standard regulatory work for the most innovative drugs in the world.
This year, the agency has looked more like a reality …