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Tag: eir

You Searched For "eir"
Ajanta Pharma Receives USFDA EIR for Paithan Plant, Inspection Closed with VAI Status

Ajanta Pharma Receives USFDA EIR for Paithan Plant, Inspection Closed with VAI Status

Parthika Patel3 July 2026 12:00 AM IST
New Delhi: Ajanta Pharma Limited has announced that it has received the Establishment Inspection Report (EIR) from the United States Food and Drug...
Zydus Wellness Expands Global Footprint with New Ireland, UAE Subsidiaries

Zydus Under USFDA Lens as Baddi Plant Receives Warning Letter

Parthika Patel4 Jun 2026 10:04 PM IST
New Delhi: Zydus Lifesciences has informed the stock exchanges that it has received a Warning Letter from the United States Food and Drug...
Granules Gets 4 USFDA Observations for US Facility

Granules Gets 4 USFDA Observations for US Facility

sheeba farhat3 Jun 2026 7:38 PM IST
New Delhi: Granules India Limited has announced that its wholly-owned subsidiary, Granules Pharmaceuticals, Inc. (GPI), located in Chantilly,...
Lupin Receives USFDA EIR for Ankleshwar Facility Following Pre-Approval Inspection

Lupin Receives USFDA EIR for Ankleshwar Facility Following Pre-Approval Inspection

sheeba farhat30 May 2026 7:10 PM IST
New Delhi: Global pharmaceutical major Lupin Limited has announced that it has received the Establishment Inspection Report (EIR) from the United...
Solara Active Pharma Gets EIR for Puducherry Ibuprofen Plant Post USFDA Inspection

Solara Active Pharma Gets EIR for Puducherry Ibuprofen Plant Post USFDA Inspection

Parthika Patel29 April 2026 4:05 PM IST
New Delhi: Solara Active Pharma Sciences Limited has announced the successful closure of a United States Food and Drug Administration (USFDA)...
Supriya Lifescience Secures USFDA EIR With VAI Status for Lote API Facility

Supriya Lifescience Secures USFDA EIR With VAI Status for Lote API Facility

MD Bureau23 April 2026 11:00 AM IST
New Delhi: Active pharmaceutical ingredients (API) manufacturer Supriya Lifescience on Wednesday announced that the USFDA has issued an Establishment...
Granules India Arm Gets USFDA VAI Status for Shamirpet Facility, No Action Required

Granules India Arm Gets USFDA VAI Status for Shamirpet Facility, No Action Required

Parthika Patel1 April 2026 5:10 PM IST
New Delhi: Granules India Limited has announced that its wholly owned subsidiary, Granules Life Sciences Private Limited (GLS), has received a...
Dr Reddys Labs Among First to Launch Generic Semaglutide in Canada

USFDA Closes Inspection of Dr Reddy's Srikakulam Facility with VAI Classification

Parthika Patel7 March 2026 8:38 PM IST
New Delhi: Dr. Reddy's Laboratories has received the Establishment Inspection Report (EIR) from the U.S. Food and Drug Administration (USFDA) for its...
Lupin Receives USFDA EIR with VAI Status for Goa Manufacturing Plant

Lupin Receives USFDA EIR with VAI Status for Goa Manufacturing Plant

Kajal Rajput27 Feb 2026 7:08 PM IST
New Delhi: Drug maker Lupin on Friday said it has received an Establishment Inspection Report (EIR) from the US health regulator for its Goa-based...
Torrent Pharma Q4 Profit Falls 27% to Rs 364 Cr Despite Strong India, US Growth

Torrent Pharma Receives USFDA Clearance for Pithampur Facility with VAI Classification

Farhat Nasim23 Nov 2024 12:49 PM IST
Mumbai: Torrent Pharmaceuticals Limited has announced that the company received an Establishment Inspection Report (EIR) from the United States...
Abacavir, Dolutegravir and Lamivudine Tablets for Oral Suspension

Lupin receives USFDA EIR for Vizag API Facility

Ruchika Sharma14 May 2020 4:19 PM IST
Mumbai: Lupin Limited has announced the receipt of the Establishment Inspection Report (EIR) from the United States Food and Drug Administration...
Dr Reddys Labs gets USFDA EIR for Srikakulam formulations plant

Dr Reddy's Labs gets USFDA EIR for Srikakulam formulations plant

Ruchika Sharma14 May 2020 11:38 AM IST
Hyderabad: Dr. Reddy's Laboratories Ltd on Wednesday said it has received an Establishment Inspection Report (EIR) from the US Food and Drug...
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