Symbiosis has dedicated suites and automation capability at our facility for the labelling and packaging of your drug products for clinical trials and niche commercial markets worldwide.
Ensuring that your final drug product is correctly labelled, packaged, shipped and stored can be a significant logistical challenge. Managing this alongside clinical trials adds additional risk as any delays at this stage can have a significant impact on the timeline for your candidate.
Once your drug product has been manufactured, we take care of preparing it for clinical or commercial use or can manage this process with your chosen partners. Our efficient clinical labelling and packaging service enables us to manage the supply chain logistics of your project and ensure that your product is delivered to your chosen location globally.
We offer exactly what you need – specialist facilities for controlled temperature and humidity storage of your medicinal product and our in-house labelling and packaging capabilities include design and sourcing services.
We have extensive experience in taking precious, complex drug products from manufacture to QP release.
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.
Extensive experience in delivering hundreds of projects allowing us to support your clinical trials.
Symbiosis can support with challenging manufacturing and handling requirements that need specialist knowledge and experience.
Overcome your development and manufacturing challenges with a partner that has the experience and capabilities to handle your highly potent ADC
Symbiosis has provided GMP manufacturing across a wide range of small molecule applications, including highly potent materials requiring specialist handling.