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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.

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.

Coater

API Facility

AFM JAPAN
Issued by Ministry of Health, Labour, Welfare, Japan Certificate No. Ag12300228
USFDA
Issued by the Department of Health and Human Services (Public Health Service, Food Drug Administration) Certificate No. FEI3009103626
EU GMP
Issued by Danish Health & Medicines Authority (A PIC/s Participating Authority) Certificate No. DK API-H 00056615
WHO GMP
Issued by Govt. of Telangana Drug Control Administration Certificate No. 10378/E(G)/TS/2016
ISO 14001 : 2004
Issued by NQA Global Assurance Certificate No.E3326
ISO 9001 : 2008
Issued by NQA Global Assurance Certificate No.18461

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.
WHO GMP
Issued by Govt. of Andhra Pradesh Drug Control Administration
EU GMP
Issued by Danish Health and Medicines Authority (A PIC/s Participating Authority) Certificate No. : DKH 00056815
WHO GMP
Issued by Govt. of Andhra Pradesh Drug Control Administration
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