Shilpa Medicare Limited
Pharmaceutical Excellence Since 1987

Shilpa Pharma Life Sciences - Unit I

World-class API manufacturing facility with 6 blocks catering to Oncology and Non-Oncology APIs with gram-to-kilo scale synthesis capabilities

39+
Years of Excellence
40+
Global Markets
500+
Product Portfolio
FDA
Certified Facilities

Advanced API Manufacturing Excellence

Shilpa Pharma Life Sciences - Unit I is our flagship API manufacturing facility strategically designed to cater to both Oncology and Non-Oncology Active Pharmaceutical Ingredients along with comprehensive CRAMS (Contract Research And Manufacturing Services) functions.

This state-of-the-art facility represents our commitment to excellence in pharmaceutical manufacturing, featuring world-class infrastructure, advanced containment technologies, and rigorous quality standards that meet global regulatory requirements.

Facility Highlights

🏭

6 Manufacturing Blocks

World-class manufacturing blocks comprising 3 dedicated Oncology blocks and 3 Non-Oncology blocks with advanced containment systems

⚗️

Large-Scale Production

Total reactor capacity of 66,000L (38,000L Non-Oncology + 28,000L Oncology) for efficient large-scale synthesis

🔬

Versatile Synthesis

Gram-to-kilo scale synthesis competence for flexible production from development to commercial scale

Global Approvals

Certified by major international regulatory authorities ensuring worldwide market access

Manufacturing Capabilities

🧬Non-Oncology APIs

  • 3 Dedicated Blocks for non-oncology product manufacturing
  • 38,000L Total Reactor Volume for large-scale production
  • Comprehensive range of small molecules to complex APIs
  • Advanced process control and automation systems

💊Oncology APIs

  • 3 Specialized Blocks with advanced containment technology
  • 28,000L Total Reactor Volume for high-potency compounds
  • Isolator technology and barrier containment systems
  • Specialized handling for cytotoxic and genotoxic compounds

CRAMS (Contract Research And Manufacturing Services)

Our Unit I facility offers comprehensive contract services from process development through commercial-scale manufacturing, providing end-to-end support for pharmaceutical companies worldwide.

Route Scouting & Process Development
Scale-Up from Lab to Commercial
cGMP Manufacturing for Global Markets

Global Regulatory Approvals

Our Unit I facility holds approval certificates from the world's most stringent regulatory authorities, ensuring our products meet the highest international quality standards:

🇺🇸
USFDA
United States
🇪🇺
EU GMP
European Union
🇦🇺
TGA
Australia
🇯🇵
PMDA
Japan
🇰🇷
KFDA
South Korea

Quality Assurance & Infrastructure

The dedicated team of professionals at Unit I, combined with our state-of-the-art infrastructure, ensures that all products are consistently delivered meeting the best industry standard quality. Our quality management system encompasses every aspect of manufacturing from raw material receipt to final product release.

Infrastructure Excellence
  • Advanced reactor systems with precise temperature and pressure control
  • Automated material handling and transfer systems
  • State-of-the-art analytical laboratories with latest instrumentation
  • Dedicated utilities and waste treatment facilities
Quality Systems
  • Comprehensive cGMP compliance across all manufacturing operations
  • Real-time monitoring and electronic batch record systems
  • Rigorous in-process and final product quality control
  • Regular regulatory audits and compliance maintenance

Strategic Location

📍Conveniently Located for Global Operations

Unit I is strategically positioned on the Hyderabad-Raichur National Highway, providing excellent connectivity for logistics and operations:

🛫 Airport Access
162 km from Rajiv Gandhi International Airport, Hyderabad
🏭 Sister Facility
Just 4 km from Raichur Unit II for operational synergy
🛣️ Highway Access
Direct access via National Highway for efficient logistics