In the wake of a German court decision that Medicines for Europe says “adopted an inordinately restrictive interpretation of the SPC manufacturing waiver,” the association has called for clarity and simplification of the SPC manufacturing waiver legislation, claiming that its use could otherwise be undermined.
A German court decision that adopted an “inordinately restrictive interpretation” of the EU supplementary protection certificate (SPC) manufacturing waiver risks undermining the use of the mechanism by European generics and biosimilars manufacturers, off-patent industry body Medicines for Europe has warned.
The SPC manufacturing waiver was hard won by the generics and biosimilars industry, allowing manufacturing for export outside the EU...
The UK regulator approved 16 medicines containing a new active substance in the first half of this year, while the European Commission issued marketing authorizations for 20 NAS-containing drugs.
Joint clinical assessment reports must be descriptive rather than reach definitive conclusions, and must not interfere with national decision making processes, according to new EU guidance.
An effort to change the US Food and Drug Administration’s conclusion that its obesity treatment candidate retatrutide is a drug and not a biologic could give the product more time with unrestricted pricing in Medicare, among other benefits.
Glenmark Pharmaceuticals agreed to pay $25m in the US to resolve its alleged liability under the False Claims Act linked to price-fixing allegations.
Revised recommendation is based on most recent data on circulating strains in US, where KP.3 is now dominant. Novavax sticks with plans targeting the JN.1 ‘parent strain.’
Pink Sheet reporter and editors discuss the US FDA’s changes to the COVID-19 vaccine indication and its revocation of the vaccine emergency use authorizations, as well as new vaccine coverage and reimbursement questions.
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