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We extracted 102 observations from 24 prospective cohort studies and 4 casecontrol studies across 15 locations (Supplementary Table 3) 117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140,141,142,143,144

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34 In January 2024, the FDA denied applications from a Chinese company, Shenzhen IVPS Tech, which argued in court that it had spent $30 million preparing its PMTA, conducted extensive testing, and provided 600,000 pages of documentation

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