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, Sharma P., and Singh R

FDA approval requires formal clinical trials, safety and efficacy review, labeling approval, and manufacturing validation under a New Drug Application (NDA) or Biologics License Application (BLA)

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Sample analysis The method was applied to A549 cells incubated in duplicate with CdCl (50 and 100 mol/L) or cisplatin (100 and 200 mol/L) for 24 and 48 h, alongside untreated controls