Delivering support through every stage of the pharmaceutical lifecycle

As leaders in API development and manufacturing, we support our customers’ projects from discovery to full commercial manufacture, while providing them access to emerging technologies, new efficiencies, and complete continuity along the way. Our customers include global pharmaceutical corporations and innovative biotechs, both of which have unique challenges and priorities at each stage of the complex molecule lifecycle. As leaders in API development and manufacturing, we support our customers’ projects from discovery to full commercial manufacture, while providing them access to emerging technologies, new efficiencies, and complete continuity along the way. Our customers include global pharmaceutical corporations and innovative biotechs, both of which have unique challenges and priorities at each stage of the complex molecule lifecycle. ... Read more

Molecule lifecycle services at Sterling

With the rising complexity of APIs in the pipeline today, complete project continuity has become increasingly critical to proactively address challenges, enhance efficiency, minimise costs, streamline development and manufacturing, and accelerate time to market. As a result, pharmaceutical and biotechnology organisations require an outsourced partner with the capabilities to support their product throughout its entire lifecycle, from grams to tonnes.

As a full service PDMO, or partnership development and manufacturing organisation, we have extensive expertise supporting our customers’ molecules from the earliest phases of discovery through to full commercial manufacture. In our global delivery network, our customers will find the world-class facilities, specialised equipment, and highly skilled team members they need to address a wide range of project requirements at every stage—all while benefiting from our simple way of working, our commitment to integrity, and our true scientific collaboration. Read less

Here’s how we accelerate your product’s path to market by delivering unrivalled support at every stage of the pharmaceutical lifecycle.

After a product moves through phase I, we continue to accelerate the development of materials for clinical trials, generate critical regulatory data, and seek new ways to enhance efficiency as the product scales up. Process optimisation remains a chief focus of our scientific and engineering teams as we help our clients prepare for phase III, and we continue to evaluate and mitigate impurities and other challenges that may arise.

Technologies & Services

Knowledge Hub Articles

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Phase Two: Molecule Lifecycle Brief

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An overview of Sterling Pharma Solutions

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API manufacturing – exploring continuous processing

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Biocatalysis webinar

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Biocatalysis whitepaper

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Biocatalysis: Using enzymes as catalysts

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Environmental sustainability in the pharmaceutical industry

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Full-lifecycle sustainability

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High Potency APIs are on the rise

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Making sense of regulatory requirements

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Making sense of hazard evaluation

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Making sense of the pharmaceutical supply chain

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Material Science at Sterling

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Meet our Solid State experts

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OncoTEX and Sterling sign clinical manufacturing agreement for development of novel treatment against ovarian cancer

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Outsourcing the development of controlled substance APIs

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Passion: What makes a PDMO?

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Positioning your HPAPI programme for success webinar

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Science: What makes a PDMO?

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Scientist Snapshot: Director of CMC, Chris Seekamp

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Scientist Snapshot: Head of Technology and Innovation, Mark Muldowney

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Service: What makes a PDMO?

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Solid form: Why is it important to consider in API development?

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Sterling partners with Newcastle University to offer PhD project

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Sterling Pharma Solutions acquires Alcami Germantown facility in US

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Sterling Pharma Solutions announces acquisition of CiVentiChem in the US

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Sterling: A journey with Chromeleon CDS

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What is a PDMO?

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Your Chromatography Data System – are you in control?