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Publications from PubMed and Web of Science that met the selection criteria but lacked corresponding registry numbers were also retained to ensure a comprehensive overview of DHT applications in rare disease trials

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Study designs often lack the rigor expected by Western regulatory standards

Furthermore, a registered API supplier on the FDAs Green List recently received an FDA warning letter for repackaging and selling substances from other sources as their own, showing that even diligent compounding pharmacies may struggle to acquire safe ingredients

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