Sterile Injectables CDMO Services, Built for Strategic Partnerships

Gloved hand lifting a filled vial from a sterile injectable filling line

At Steriscience, we are a specialized sterile injectables CDMO, providing end-to-end development and manufacturing services while building select B2B partnerships with pharmaceutical and biotech companies worldwide. Our technical expertise, regulatory capabilities, and world-class manufacturing infrastructure help customers accelerate development, ensure reliable supply, and bring high-quality products to global markets.

From concept to commercialization, we provide the infrastructure, expertise, and partnership needed to navigate complexity with confidence.

2020Year of incorporation
2Manufacturing plants
15Products

Advancing Access Through Manufacturing Excellence

Our robust manufacturing capabilities support the development and production of essential hospital medicines across a wide range of differentiated sterile injectable delivery platforms. With a strong focus on quality, compliance, and supply reliability, we help our partners deliver life-changing therapies where they are needed most.

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Scientist examining a sample under a microscope in the Steriscience laboratory
Gloved hands using a pipette to transfer a sample during formulation development

Your Partner Across the Product Lifecycle

From generic product development and ready-to-use (RTU) conversions, including 505(b)(2) pathway support, to technology transfer, scale-up, validation, and commercial manufacturing, Steriscience delivers integrated CDMO solutions tailored to your needs.

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One Partner. One Process. One Path to Market.

Feasibility & Development

Generic product development, formulation science, and RTU conversions.

Technology Transfer

Seamless transition from your site or third-party to ours.

Regulatory Support

We provide in-house regulatory support to ensure compliance, with assistance in documentation and regulatory submission.

Commercial Scale-up

Full commercial manufacturing with dedicated project management.

Process Validation

Rigorous PV batches across all formats and scales.

Quality-Driven Compliance

Robust QMS, GMP audits, and batch release built into every stage.

One partner, from development through commercialization

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