Symbiosis specialises in the production of injectable pharmaceuticals for clinical trials and low volume commercial supply. Our GMP-compliant manufacturing facility is fully licensed by the MHRA so rest assured, you’re in safe hands.
We provide an integrated range of services, which allows our clients to get their drug product manufactured, tested, labelled and packaged, stored, distributed and QP released quickly and efficiently. Additionally, our experienced project management team offers a single point of contact throughout each project, which ensures we communicate with you clearly and as frequently as you need.
Read more about our services below and see whether we can support your drug manufacturing project.
Sterile Fill Finish
Operating from our state-of-the-art site in Scotland, we are licensed for the sterile filling of liquid and lyophilised investigational medicinal products (IMPs). Sterile manufacturing is at the core of what we do, so we can assist if you require the supply of drug products for pre-clinical, clinical trials and low volume commercial markets.
DRUG PRODUCT TESTING
Complementing our sterile manufacturing capability, our expert team can also manage and coordinate all of your analytical and microbiological testing requirements. This allows you to keep your drug product in the hands of one reliable partner and ensures your batch is delivered in a speedy manner.
Clinical Labelling & Packaging
We have dedicated rooms at our facility for the labelling and packaging of drug products for clinical trials and niche commercial markets worldwide. Our efficient service ensures we manage the supply chain and logistics of your project to ensure it is delivered to your chosen location, without fail.
Qualified Person Release
Our quality experts release clinical batches under our MHRA IMP license and commercial licensed products under a commercial manufacturer/importer’s license. Manufacturing to GMP regulations, we support QP release to clinic, market or direct to you for onward processing.
Symbiosis is able to assist with a range of product development services to get products from the pre-clinical phase into clinical trials. So if you’re at the pre-manufacturing stage, we can support you with formulation development, lyophilisation cycle development and process development expertise.