We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
A new EU safety net for snaring illicit drugs went into effect on Feb. 9 — but the UK may not be under its protection for very long, according to the Association of the British Pharmaceutical Industry (ABPI). Read More
In a first-of-its-kind action, the Department of Justice filed suit against two Tennessee pharmacies to prevent them from dispensing opioids. Read More
Pfizer asked the FDA to clarify the term “total content” in its draft guidance for biosimilar development, for demonstrating that a drug and a reference product have the same strength. Read More
Australia’s Therapeutic Goods Administration (TGA) is asking for feedback on changes it’s considering for its generic drug market authorization process — including the potential use of foreign reference products to show bioequivalence. Read More
Petitions aimed at delaying approvals of competing drugs are diverting resources away from the agency’s public health efforts, the FDA said in a report to Congress. Read More