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Regulatory bodies, including the FDA and EMA, require comprehensive immunogenicity testing during clinical development, including method validation, sample handling, and data traceability
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[email protected] *Kyong Yeun Jung and Kyoung Min Kim contributed equally to this study as first authors
R., Blonde, L
The wide variance probably is because some papers have only looked at macroscopic while others have reported both micro and macroscopic Melanosis Coli
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