our services

CDMO Services

CDMO Services

At Anugraha Lifescience, our CDMO services provide seamless support from early process development to multi-ton commercial manufacturing. Whether it’s a milligram-scale trial batch or large-scale production, we offer both GMP and non-GMP manufacturing capabilities to meet your specific needs.

Our expertise spans APIs, Key Starting Materials (KSMs), Registered Starting Materials (RSMs), and Intermediates, ensuring a truly end-to-end solution for pharma and specialty chemical partners worldwide.

Key Features & Capabilities:

State-of-the-Art Manufacturing Facility

  • Built on several acres of strategically located land near Bengaluru, ensuring supply chain efficiency
  • Equipped with GLR and SSR reactors ranging from 650 L to 5 KL, pilot plant, and kilo-lab facilities
  • GMP-level quality systems and Class 1,00,000 cleanrooms for regulated manufacturing
  • Modern utilities, waste treatment, and EHS-compliant systems for sustainable operations

Process Development & Optimization

  • Route scouting and identification of cost-effective, non-infringing synthetic pathways
  • DoE/QbD-based optimization to maximize yield, purity, and process robustness
  • Development of reproducible, scalable processes suitable for commercial production
  • Application of green chemistry practices and process safety assessments

Scale-Up & Technology Transfer

  • Smooth transition from mg → g → kg → multi-ton manufacturing
  • Pilot trials to de-risk commercial production
  • Comprehensive tech transfer packages with process flow diagrams, risk assessments, and batch records
  • Validation protocols to ensure consistency, impurity control, and regulatory compliance

Regulatory & Documentation Support

  • Preparation of DMF-ready documentation (US, EU, Japan, ROW)
  • Batch manufacturing records, SOPs, change controls, and deviation tracking
  • Full traceability and audit readiness for client or regulatory inspections
  • Strict IP protection and NDA-driven project execution

Commercial Manufacturing of APIs & Intermediates

  • Consistent, large-scale production under robust quality management systems
  • On-time delivery of APIs, intermediates, KSMs, and RSMs for global partners
  • Lifecycle management with continuous process improvement and cost optimization

Non-Pharma Material Support

Beyond pharmaceuticals, we also offer custom manufacturing for non-pharma materials such as:

  • Fine and specialty chemicals
  • Agrochemical intermediates
  • High-purity chemicals for industrial and research use
  1. Dual GMP & non-GMP manufacturing streams
  2. Proven capability to handle complex chemistries safely
  3. Seamless integration with our R&D and analytical capabilities
  4. Flexible engagement models — from FTE to project-based execution
  5. Trusted by clients across Japan, Europe, Latin America, and Russia