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Shilpa Biologicals Opens Manufacturing Site for Fully Integrated ADC Development

The new bioconjugation site completes the CDMO’s capabilities across payload, linker, and Mab, with onboarding set to start in September.

By: Rachel Klemovitch

Assistant Editor

Shilpa Biologicals, a full-service CDMO, opened a dedicated bioconjugation suite at its Dharwad, India site. The suite is currently undergoing validation and is expected to begin onboarding client programs by September 2025.

The new multi-client bioconjugation suite is built to support the manufacture of ADCs and other advanced bioconjugates. It includes 200L single-use bioconjugation reactors and a lyophilization capacity of up to 65 kg. 

Complementary development laboratories will provide process development, analytical characterization, and early and late-stage scale-up capabilities. For final dose requirements, Shilpa’s Hyderabad site is also equipped with multiple isolator-based fill-finish lines dedicated to cytotoxic products.

The facility is located next to the company’s existing commercial biologics manufacturing facility.

This latest expansion positions Shilpa Biologicals among a select group of global CDMOs capable of providing clinical and commercial-scale manufacturing across three core antibody-drug conjugate (ADC) components.

Shilpa Biologicals, Chief Executive Officer Dr. Sridevi Khambhampaty commented, “Our co-located ADC services — spanning payloads, linkers, antibodies, and bioconjugation — are generating significant industry interest, especially from US and European biotech companies seeking a single, reliable partner to support their journey from discovery to commercial launch.”

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