Sterile Biopharmaceutical Manufacturing Specialists

We offer you rapid access to fill-finish slots for your injectable drug products at clinical and commercial scale.

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We specialise in the GMP manufacture of liquid and lyophilised biological and small molecule drug products

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ATMPs/Viral Vector Therapies

Clinical and small scale commercial manufacturing of advanced therapeutics such as viral vectors for cell and gene therapies, oncolytic viruses and critical raw materials such as plasmids.

RNA and Peptide Therapies

Symbiosis can support with challenging manufacturing and handling requirements that need specialist knowledge and experience.

Antibody-Drug Conjugates

Overcome your development and manufacturing challenges with a partner that has the experience and capabilities to handle your highly potent ADC

mAbs and Recombinant Therapies

Extensive experience in delivering hundreds of projects allowing us to support your clinical trials.

Small Molecule

Symbiosis has provided GMP manufacturing across a wide range of small molecule applications, including highly potent materials requiring specialist handling.

Vaccines

Supporting clinical batches across traditional attenuated or inactivated products to recombinant, viral vector and nucleic acid based vaccine technologies.

About Us

Symbiosis Pharmaceutical Services is a world-class fill-finish CDMO, based in Stirling, UK and we offer our clients rapid access to GMP sterile fill-finish manufacturing slots for clinical trial and commercial scale.

Operational flexibility and regulatory compliance are at the core of Symbiosis and as a global biologics CDMO, we have world class expertise and experience across a full range of biologics, including ATMPs, mAbs and ADCs. We also specialise in the manufacture of small molecules.

Our services include:

* Sterile GMP manufacturing
* QC inspection
* Analytical testing
* Labelling and Packaging
* QP Release
* Temperature-controlled storage and shipment

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Resources

See our latest news, resources and upcoming events.

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9th June 2026

Regulatory Capabilities Factsheet

Learn how Symbiosis can help you navigate the regulatory environment when manufacturing your drug product for clinical trial or commercial ...

7th June 2026

Aseptic Manufacturing Capabilities Sheet

Learn about our automated fill-finish capabilities and batch capacity in this aseptic capabilities sheet.

31st May 2026

Symbiosis in the Spotlight: BioPharma Boardroom Interview

Our Chief Operating Officer, David McClelland, recently sat down with BioPharma Boardroom to discuss how Symbiosis is strategically scaling to ...

8th September 2026 to 9th September 2026

Nordic Life Science Days 2026

Meet Symbiosis at the Nordic's leading life science partnering event in Stockholm, Sweden - 8th - 9th September 2026.

30th April 2026

CPHI Online - An Interview with Joanne Anderson

CPHI Online, the global community for the pharmaceutical industry, recently spoke with Symbiosis Chief Commercial Officer Joanne Anderson, to get ...

31st March 2026

Symbiosis Expands Commercial Capabilities with Addition of New Stability Chamber

Symbiosis has expanded its Quality Control (QC) laboratory with the installation of a new 30°C stability chamber. This addition enables ...

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Take a virtual guided tour of our GMP sterile manufacturing facility to see how we handle your precious drug from receipt to dispatch.

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