Shilpa Pharma is a leading Contract Development and Manufacturing Organization (CDMO) in India, delivering high-quality, end-to-end solutions for pharmaceutical innovators worldwide. With decades of expertise in oncology APIs, formulations, peptides, polymers, and biologics, we support clients at every stage—from early development to commercial-scale manufacturing. Our comprehensive CDMO services include formulation development, process optimization, analytical support, and scalable manufacturing, ensuring a seamless transition from concept to market-ready products.
Backed by state-of-the-art, regulatory-compliant facilities and a team of 100+ R&D specialists along with 1500+ skilled professionals, Shilpa Pharma combines scientific excellence with operational reliability. Our commitment to innovation, quality, and efficiency makes us the trusted partner for pharmaceutical companies seeking flexible, scalable, and reliable solutions for drug development and manufacturing.
From simple to multi-step syntheses, we deliver precision-built CDMO solutions tailored to your needs.
Expertise in solid and solution-phase synthesis, cryogenic, and high-pressure reactions.
Offering non-GMP to GMP manufacturing — from lab-scale to commercial production.
Leading the Way in Pharma Innovation
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At Shilpa Pharma, our custom manufacturing services are designed to deliver precision, quality, and compliance at every stage. Equipped with cutting-edge technology and certified by leading regulatory authorities, our facilities handle everything from raw material sourcing to final packaging under strict quality protocols.
We go beyond just meeting standards — we ensure international benchmarks are exceeded, enabling you to bring safe, effective, and high-quality products to the global market with confidence.
Key Highlights:
At Shilpa Pharma, our custom development services are focused on creating innovative, compliant, and scalable pharmaceutical solutions tailored to your needs. Leveraging advanced R&D capabilities and GMP-certified facilities, we support every stage — from route scouting and process optimization to formulation development and pilot-scale manufacturing.
We ensure that your products meet not just regulatory standards but also global quality expectations, helping you bring safe, effective, and market-ready medicines to patients worldwide.
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