 "Lupin")
Drug maker Lupin on Monday said it has received an establishment inspection report (EIR) from the US health regulator for its inhalation research centre in Florida.
The facility was inspected by the US Food and Drug Administration (USFDA), between February 19, 2020, and February 26, 2020, on behalf of the UK Medicines and Healthcare Products Regulatory Agency (UKMHRA) for company's application for generic Fostair.
"The receipt of the EIR with satisfactory voluntary action indicated' status validates our commitment towards ensuring the highest levels of quality and current good manufacturing practice compliance at all our sites," Lupin Ltd CEO Vinita Gupta said in
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