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They would need to query ClinicalTrials.gov, pull pharmacology data from ChEMBL, run FAERS disproportionality analyses, compile and standardize clinical efficacy data across trial designs, build patent landscape timelines, and synthesize everything into a strategic framework with actionable recommendations
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Nature 591(7851):551563
Salegio EA, Streeter H, Dube N et al (2014) Distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: implications for gene and drug therapy
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