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Consequently, we performed a comprehensive assessment and characterization of all new molecular entities, therapeutic biologics, and gene and cell therapies approved via the FDA due to the fact 1980. Additionally, we analyzed the approval pathways and regulatory designations inside the context on the legislative and regulatory landscape while in th
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We also gathered information regarding notices of FDA regulatory steps accessible with the Federal Register22 and also the therapeutic class in the WHO Anatomical Therapeutic Chemical Classification System23 (Supplemental Table S1). We labeled the medicine using the anatomical key group. We chose the therapeutic subgroup for systemic anti-infective