🎯 Objective:

To bridge Indian CDMO partners with global and domestic pharmaceutical/biotech companies seeking high-quality, cost-effective development and manufacturing solutions.

​​🧬 Why Partner with Indian CDMOs?

✅ Globally Compliant Facilities
→ USFDA, EU GMP, WHO PQ, ANVISA, and MHRA-approved sites

✅ Cost-Efficient Excellence
→ Competitive pricing without compromising quality or timelines

✅ Rich Scientific Talent Pool
→ Skilled experts in API synthesis, formulation science, and regulatory affairs

✅ End-to-End Services
→ From pre-clinical development to commercial-scale manufacturing

✅ Successful Global Track Record
→ Proven delivery to global markets including the US, Europe, LATAM, Africa, and SEA

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​🔍 Explore CDMO Capabilities

🏭 Services Offered:

• ⚗️ API Development & Commercial Manufacturing

• 💊 Formulation R&D (Orals, Injectables, Topicals, etc.)

• 🧪 Analytical Method Development & Validation

• 🧫 Stability Studies & ICH-Compliant Documentation

• 🔁 Tech Transfer & Scale-Up Support

• 📋 Regulatory Filing Support (DMF, ANDA, CTD, eCTD)

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🏅 Featured Indian CDMO Partners

Discover pre-vetted, reliable CDMOs with:

• ✔️ Specialized therapeutic expertise (Oncology, CNS, Cardio, etc.)

• ✔️ Advanced facilities & manufacturing technologies

• ✔️ Integrated project management systems

• ✔️ Transparent communication & milestone tracking

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