Shilpa Medicare Limited
Precision Medicine
Innovation

End-to-End ADC Development, Engineered for Speed and Scalability

Advanced pharmaceutical solutions

Targeted • Precise • Effective

A Single-Source CDMO Partner Accelerating Your Antibody Drug Conjugate from Concept to Commercial Supply

Peptides
Custom synthesis
Polymers
Drug delivery
ADCs
Targeted therapy
End-to-End ADC Development, Engineered for Speed and Scalability
1000+
Peptides Synthesized
50+
Polymer Types
200+
ADC Projects
99.5%
Purity Standard

End-to-End ADC Development, Engineered for Speed and Scalability

Antibody Drug Conjugates demand a rare combination of expertise — complex small-molecule chemistry, biologics development, high-potency containment, and tightly controlled conjugation processes. Most ADC programs lose time and capital coordinating these capabilities across multiple vendors.

At Shilpa Biologics and Shilpa Pharma Lifesciences, we eliminate that fragmentation. Our fully integrated ADC platform brings payloads, linkers, antibodies, conjugation, analytical characterization, and GMP manufacturing into a single, accountable partnership — so your molecule moves faster, with fewer hand-offs, and with global regulatory readiness built in.

Core ADC Services

ADC Process Development

Rigorous QbD-driven development ensuring scalable and reproducible processes

Conjugation Optimization

Consistent DAR control and reduced heterogeneity across Lysine and Cysteine platforms

Payload-Linker Development

Deep synthetic chemistry expertise with a broad portfolio of cytotoxic payloads

Analytical Characterization

Comprehensive analytics from DAR determination to disulfide mapping

GMP Manufacturing

Purpose-built isolator-based facilities for highly potent ADC production

Fill-Finish & Lyophilization

Sterile fill-finish and lyophilization cycle development under aseptic conditions

Technology Transfer

Structured tech transfer protocols with full documentation support

Scale-Up & Process Validation

From pilot to commercial scale with regulatory-ready validation packages

Development Stages Supported

Discovery Support

Early-stage candidate evaluation and feasibility

Preclinical Development

Non-GMP to GMP transition with full analytics

Clinical Manufacturing

Phase I–III supply with regulatory documentation

Commercial Supply

Validated, scalable processes for market launch

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