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Lupin gets USFDA EIR for Ankleshwar unit
The inspection of the facility was conducted from August 16-19, 2022.
Mumbai: Global pharma major Lupin Limited has announced that the Company has received the Establishment Inspection Report (EIR) from the United States Food and Drug Administration (USFDA) for its Ankleshwar manufacturing facility, located in Gujarat, India.
The inspection of the facility was conducted from August 16-19, 2022.
Commenting on the development, Nilesh Gupta, Managing Director, Lupin, said, "We are very happy to have received the EIR for our Ankleshwar facility from US FDA. We remain committed to enhancing compliance and quality standards across all our manufacturing sites."
Read also: Lupin unveils generic equivalent of Revatio for Oral Suspension in US
Ruchika Sharma joined Medical Dialogue as an Desk Editor for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751