British Columbia’s recently-announced initiative to switch patients using biologic drugs to biosimilar equivalents has prompted “concerns” from patients and doctors, according to originator-backed lobbying group the Alliance for Safe Biologic Medicines.
ASBM Hits Back At British Columbia Switching Scheme
Originator-backed lobbying group the Alliance for Safe Biologic Medicines has raised concerns over a biosimilar switching policy recently unveiled by the Canadian province of British Columbia.

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FDA staffing cuts are making negotiation preparations more difficult, but also could mean the result is a smaller user fee renewal package.
The US FDA has deemed certain CRO Raptim Research’s in vitro bioequivalence studies as “not acceptable” and raised concerns over its in vivo study methods. Will other agencies follow suit?
The EMA has accepted for review Henlius’ Perjeta biosimilar, which is to be commercialized by the Chinese company’s global partner Organon in the EU.