Blue Hawk Life Sciences is a GMP-certified pharmaceutical manufacturer specialising in pellet-based dosage forms — enteric-coated, sustained-release, immediate-release, and dual drug-release systems.
Blue Hawk Life Sciences Pvt. Ltd. initiated with the acquisition of land at I.P. Cherlapally, Hyderabad — construction and fit-out commenced.
Formulations R&D fully operational. New products developed and placed under stability studies.
Production facility commissioned. Water validation completed. Manufacturing License application submitted to Telangana State Drug Authority.
Manufacturing License officially granted — commencement of commercial production.
Additional products added to the manufacturing license scope, bringing the licensed portfolio to 19 products.
GMP Certificate approved and issued. Facility is fully GMP certified and compliant.
Founded in 2021 and operational since 2025, Blue Hawk Life Sciences Pvt. Ltd. is a dedicated pharmaceutical manufacturer based in Hyderabad, Telangana. We specialise in pellet-based pharmaceutical intermediates — enteric-coated, sustained-release, immediate-release, and dual drug-release systems.
Our 30,000 sq ft facility is built to strict Schedule M standards, equipped with state-of-the-art PLC-controlled Wurster coaters ensuring precision manufacturing with minimal manual intervention. We hold a GMP certificate and are WHO-GMP and Schedule M compliant.
Guided by a leadership team with decades of combined pharmaceutical, regulatory, R&D, and operational expertise, our goal is to become the most respected name in pharmaceutical pellet and granule formulations — supplying high-quality, competitively priced products to pharma companies globally.
GMP certified facility. Full Schedule M and WHO-GMP compliance embedded into every process.
Dedicated Formulations R&D and Analytical R&D labs. R&D Head with 11+ years of OSD experience leading pre-formulation, process optimisation, and technology transfer.
30+ employees across QA, QC, Production, R&D, and Engineering. Plant Head with 24 years of pharma experience; QA Manager with 17+ years of regulatory expertise.
All employees sign NDAs and pledge strict confidentiality. We operate with transparency and ethical business practices at every level.
Core of our pellet manufacturing — high-capacity, fully automated PLC-controlled systems.
Full suite of GMP-grade equipment for blending, sizing, coating, and drying.
Dedicated in-house R&D wing for new product development and technology transfer to production.
Comprehensive analytical infrastructure delivering reliable test data for every batch.
Robust QA system ensuring end-to-end documentation, compliance, and product integrity.
ISO 8 (Class 1,00,000) classified cleanrooms with validated purified water and HVAC infrastructure.
GMP certified. Schedule M and WHO-GMP compliant facility.
Across 9 departments — production, QA, QC, engineering, R&D, warehousing, and more.
Class 1,00,000 classified production areas with ≥25 air changes/hour and validated HVAC.
Products manufactured to Indian, US, and British Pharmacopeial standards as applicable.
Plot No. 203/6, Phase-II, Sector-III,
I.P. Cherlapally, Hyderabad,
Telangana – 500 051