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Natco Pharma gets EIR from USFDA on pharmacovigilance requirements

Natco Pharma gets EIR from USFDA on pharmacovigilance requirements
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Lupin receives Establishment Inspection Report from USFDA for its Aurangabad manufacturing facility

The inspection was conductedfrom March 6 to March 15, 2024. The U.S. FDA has determined that the inspection classification ofthe facility is Voluntary Action Indicated (VAI)

Small-cap Shares Fall Sharply - Monday Closing Report

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