Can anyone share how they have tackled their LASA policy/lists when it comes to addressing biosimilars and monoclonal antibodies. We think the nomenclature is easily confused and are evaluating possible safety impacts/look-alike, sound-alike risks as more of these products come to market. We would prefer to avoid blanket statements such as adding all monoclonal antibodies are at risk for LASA errors.
Thanks!
Tue, 12/12/2023 - 09:59
#1
LASA Policy/ list updates for Biosimilars/ Monoclonals