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Indian drug plants supplying half U.S. generics face FDA probe over falsified data, poor conditions, and patient deaths.
Indian pharmaceutical plants supplying nearly half of America’s generic drugs are under investigation after reports reveal widespread data falsification, document destruction, and poor manufacturing conditions.
Based on FDA records and on-site visits in Telangana, investigators found repeated violations including falsified lab results, unsanitary environments, and efforts to conceal evidence.
Former FDA inspector Peter Baker stated that substandard production is common despite strong documentation and confirmed patient deaths linked to faulty drugs.
The findings raise serious concerns about the safety of the U.S. drug supply chain, highlighting systemic flaws in oversight and accountability.
Las plantas farmacéuticas indias que suministran la mitad de los genéricos estadounidenses enfrentan una investigación de la FDA por datos falsificados, malas condiciones y muertes de pacientes.