Sterile liquid pharmaceutical manufacturing facility with fill-finish and lyophilization equipment
Injectable Manufacturing

Advancing Sterile Liquid Development: Enabling Integrated Solutions for Small Molecules and Biologics

PCI Pharma Services
Injectable Manufacturing

Site expansions in the United States and Europe are central to a vision of integrated sterile development.

Anshul Gupte, PhD, VP of Pharmaceutical Development at PCI Pharma Services, discusses sterile manufacturing expansions and the value of co-locating development centers of excellence within GMP sterile facilities.

Anshul Gupte, PhD, VP of Pharmaceutical Development at PCI Pharma Services, discusses sterile manufacturing expansions and the value of co-locating development centers of excellence within GMP sterile facilities.

Co-Locating Development and Manufacturing

Placing development centers of excellence inside GMP sterile facilities reduces technology transfer risk and accelerates time to market.

Small Molecules and Biologics

Integrated capabilities allow a single partner to support both modalities from formulation through fill-finish.

Lyophilization Development

Dedicated lyophilization development, including for ADCs, builds robust cycles that scale to commercial manufacturing.

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