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Approvals
Lee Pharma Limited was established in 1997 in India it is a research-driven company with a critical focus on the development, synthesis, and commercialization of new products and cost-effective processes.
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We manufacture several intermediate chemicals, Active Pharmaceutical Ingredients & Semi-finished Dosage Forms (Pellets & Granules), and Finished Formulations. Our expertise in the field won us, numerous clients, in India as well as across the globe.
Lee Pharma Manufacturing facilities are approved by several international regulatory bodies such as USFDA, EUGMP, WHO GMP etc.
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API Facility
AFM JAPAN | Issued by Ministry of Health, Labour, Welfare, Japan
Certificate No. Ag12300228
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USFDA | Issued by the Department of Health and Human Services
(Public Health Service, Food Drug Administration)
Certificate No. FEI3009103626
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EU GMP | Issued by Danish Health & Medicines Authority
(A PIC/s Participating Authority)
Certificate No. DK API-H 00056615
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WHO GMP | Issued by Govt. of Telangana Drug Control Administration
Certificate No. 10378/E(G)/TS/2016
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ISO 14001 : 2004 | Issued by NQA Global Assurance Certificate No.E3326
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ISO 9001 : 2008 | Issued by NQA Global Assurance Certificate No.18461
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Pellets Facility
Finished Formulation Facility
EU GMP | Issued by Hungarian Authority - National Institute of Pharmacy & Nutrition (A PIC/s Participating Authority)
Certificate No. : OGYEI/38395-4/2020.
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WHO GMP | Issued by Govt. of Andhra Pradesh Drug Control Administration
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EU GMP | Issued by Danish Health and Medicines Authority (A PIC/s Participating Authority)
Certificate No. : DKH 00056815
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WHO GMP | Issued by Govt. of Andhra Pradesh Drug Control Administration
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