Manufacturing ExcellenceFor Quality Oncology
Building sustainable, world-class pharmaceutical infrastructure for affordable cancer medicines—from Hyderabad to the world.
Current Operations
Our Hyderabad headquarters and trusted manufacturing partners enable us to deliver quality oncology medicines today.
Corporate Office & Operations
Our corporate headquarters manages business operations, quality oversight, regulatory affairs, and product development coordination.
Key Functions:
WHO-GMP Certified Manufacturing Partners
We work with qualified contract manufacturing organizations (CMO) that meet international quality standards for oncology pharmaceutical production.
Manufacturing Capabilities
- Sterile injectable manufacturing with cytotoxic containment
- Oral solid dosage (tablets and capsules)
- High-potency API handling
- WHO-GMP certified facilities
- Full quality control laboratories
- Regulatory-compliant batch documentation
Strategic Advantages
- Access to specialized oncology manufacturing infrastructure
- Flexible production capacity for market growth
- Established quality systems and regulatory compliance
- Experienced technical teams
- Cost-effective production for competitive pricing
Integrated Manufacturing Campus
A 5-acre state-of-the-art pharmaceutical campus in Telangana—designed for sustainability, quality, and international compliance.
Integrated Manufacturing Campus
A state-of-the-art integrated pharmaceutical campus designed to WHO-GMP, US FDA, and EMA standards with sustainability at its core.
Manufacturing Capabilities
Compliance & Sustainability
Why Our Integrated Campus?
Vertical Integration
Control the entire value chain from API to finished product, ensuring quality and reducing costs
Regulatory Readiness
Designed from day one for WHO, FDA, and EMA inspections with international compliance built in
Sustainability Leadership
Solar power and zero discharge make us an environmentally responsible pharmaceutical manufacturer
Speed to Market
In-house capabilities eliminate third-party dependencies and accelerate product launches
Cost Efficiency
Integrated operations and renewable energy reduce manufacturing costs for affordable medicines
Quality Assurance
Direct oversight of every production step ensures consistent, high-quality oncology medicines
Campus Highlights
Modern infrastructure combining pharmaceutical excellence with environmental sustainability
Solar Power
100% renewable energy with rooftop and ground-mounted solar panels for sustainable operations
Zero Liquid Discharge
Advanced effluent treatment system with water recycling and zero environmental impact
API Manufacturing
In-house oncology API production with high-potency compound isolation and containment
Sterile Injectables
State-of-the-art aseptic filling suite with cytotoxic containment for oncology injectables
Oral Solid Dosage
Modern tablet and capsule manufacturing with dedicated high-potency lines
Quality Control
Fully equipped analytical laboratories with HPLC, GC, dissolution, and microbiology
Design & Compliance Standards
Built to international pharmaceutical manufacturing standards from day one
Regulatory Compliance
- WHO-GMP (World Health Organization Good Manufacturing Practice)
- US FDA 21 CFR Parts 210, 211 (Current Good Manufacturing Practice)
- EMA Annex 1 (Manufacture of Sterile Medicinal Products)
- ICH Q7 (Good Manufacturing Practice for APIs)
- Schedule M (India CDSCO requirements)
Safety & Containment
- Cytotoxic drug handling (OEB 4-5 containment)
- HVAC systems with HEPA filtration
- Differential pressure cascades
- Airlocks and gowning areas
- Segregated waste management
- Environmental monitoring
Environmental Sustainability
- Solar power generation (100% renewable)
- Rainwater harvesting
- Zero liquid discharge effluent treatment
- Energy-efficient HVAC and lighting
- Green building materials
- ISO 14001 Environmental Management System
Quality Systems
- Computerized quality management system (QMS)
- Electronic batch manufacturing records (eBMR)
- 21 CFR Part 11 compliant data integrity
- Validated analytical methods
- Stability chambers (ICH conditions)
- Microbiology laboratory (sterility, endotoxin)
Development Timeline
From planning to production—our phased approach to building world-class infrastructure
Planning & Design
Current- Land acquisition and site selection
- Architectural and engineering design
- Regulatory pre-submission consultations
- Environmental impact assessment
- Financial planning and fundraising
Construction
Future- Site preparation and infrastructure
- Building construction (API, injectables, oral)
- HVAC, utilities, and support systems
- Solar power installation
- Effluent treatment plant
Validation & Commissioning
Future- Equipment installation and qualification (IQ/OQ/PQ)
- Process validation studies
- Analytical method validation
- Cleaning validation
- Environmental monitoring validation
- Mock batches and stability studies
Regulatory Approval & Launch
Future- WHO-GMP inspection and certification
- CDSCO approval for commercial manufacturing
- FDA pre-approval inspection (PAI)
- EMA inspection (if applicable)
- Commercial production launch
Partner in Our Growth
Learn more about our manufacturing capabilities, campus plans, or partnership opportunities.
Business Inquiries
Discuss manufacturing partnerships, CMO services, or facility tours
Technical Details
Request campus specifications, compliance documents, or facility capabilities