Partners for Life

Delivering recombinant proteins, viral vaccines and gene therapies to patients requires commitment and partnership. As a CDMO our focus is to combine technical leadership in cell culture, microbial fermentation and viral vectors with world class GMP manufacturing facilities to advance tomorrow’s medicines.

25+ Years of Experience

What We Do

Formulation Development

Balancing the need for speed with robust science with comprehensive and modern analytical and formulation capabilities and technical expertise
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Saturn

A Monoclonal Antibody Platform for reliable delivery of mAb based therapeutics
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Apollo Mammalian Expression

A Mammalian Expression Platform developed for robust, high levels of monoclonal antibody expression designed with manufacturability for the entire life of your product
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Paveway Microbial Expression

Incorporating key aspects for the delivery of an E.coli based expression process with industry leading titers and suitable for large-scale manufacture using antibiotic-free fermentation
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Gene Therapy

Delivering scalable Gene Therapy processes.
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Thought Leadership

You are about to embark on a clinical journey—be it early, pre-clinical investigation or a later phase of the product lifecycle—it’s good to know Thought Leaders are paving the way.
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Featured
brochures
publications
case-study
whitepaper
Brochure

Apollo Mammalian Expression Platform

Learn how we can produce a high quality recombinant cell line to take your biopharmaceutical from pre-clinical through to commercial production with the use of our Apollo™ mammalian expression platform.

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Brochure

pAVEway Advanced Microbial Expression Platform

Learn more about our innovative microbial expression system for large-scale production of antibiotic-free therapeutic proteins.

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Brochure

Viral Products Brochure

Learn more about our Viral Products Expertise Experience & Capabilities

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Publications

Designing and Operating Flexible Advanced Therapies Manufacturing

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Publications

Mass Spectrometric Conjugate Characterization: Process Qualification of Recombinant Protein–Hapten Conjugation

Here we present case studies in development of reliable methods based on mass spectrometry (MS) to characterize a protein–hapten drug substance during late-phase process validation. This protein is modified by succinylation to enable conjugation with an aminated hapten.

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Publications

Rapid Development of High-Quality, Robust Mammalian Cell Culture Manufacturing Processes

Learn the approach that our scientists uses to accelerate the development process from gene to finish by shortening the timeline, incorporating quality by design (QbD) principles, and designing the process to be as robust as possible.

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Case Study

Case Study #5 – Expanding Single-Use Biomanufacturing

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Case Study

Case Study #4 – Single-Use Biologics Manufacturing for Long Term Needs

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Case Study

Case Study #3 – Assess Biologics Manufacturing Needs

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Whitepapers

Three steps to start you on the path to obtaining the ‘best’ recombinant CHO cell line

The keys to developing biomanufacturing processes which are efficient, robust and of high quality start during cell line and process development.

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Whitepapers

Xtalks from gene to manufacturing

Application of efficient cell line development strategies to deliver reliable, high quality biomanufacturing processes

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Whitepapers

pAVEwayTM expression system for the efficient expression of therapeutic proteins

The Escherichia coli pAVEwayTM expression system described here has been developed to ensure high product titres and efficient scale up to GMP manufacture, whilst minimizing many common issues seen in other expression systems, such as ‘leaky’ expression (expression of recombinant protein in the absence of inducer).

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