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., aggregation, fragmentation, charge/size variants, subvisible particles, surface interactions) to inform formulation and processdesigndecisions. Identifyand address technology gapsimpactingbiologics stability
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., aggregation, fragmentation, charge/size variants, subvisible particles, surface interactions) to inform formulation and processdesigndecisions. Design, develop, and execute automated high-throughput formulation
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conditions. Investigate ADC- and biologics-relevant CQAs (e.g., aggregation, fragmentation, drug-to-antibody ratio, free payload, charge/size variants, subvisible particles, surface interactions) to inform
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