
We are experts in Outer Membrane Vesicles (OMVs) production, providing end-to-end services from early-stage development to large-scale manufacturing. Our capabilities include upstream and downstream processing, as well as formulation development. By optimizing fermentation conditions and purification processes, we ensure the production of high-quality, high-yield OMV products for therapeutic and vaccine applications.
Comprehensive OMVs production services, from research to GMP clinical trial manufacturing.
Flexible manufacturing capabilities, supporting both small-scale research batches and large-scale clinical production.
Tailored OMVs solutions to meet the specific research or clinical trial requirements.
Efficient processes that ensure rapid production timelines without compromising quality.
High-quality OMVs production for both research applications and GMP-compliant clinical use.
In-process analytics, final release and stability testing.
Use of biopharmaceutical-grade raw materials, including animal-free origin.
Comprehensive documentation and compliance guidance, ensuring a fully compliant CMC package for regulatory submissions and clinical trial applications.

We provide high-quality OMVs for preclinical studies, ensuring the production of functional vesicles that are optimized for therapeutic and vaccine research. Our solutions include small-scale cultivation, customized purification methods and formulation to meet the specific needs of preclinical testing.
Small-scale cultivation and expression studies
OMV purification and analytical characterization
Flexible small-scale production capabilities
Custom formulation and stability testing
Process optimization for improved efficiency and results
We offer GMP-compliant OMV production for clinical trials, ensuring consistent quality and regulatory compliance. Our process is designed for scalable production, with robust quality control and documentation to meet clinical trial standards.
Clinical-grade cultivation and expression studies
OMV purification with regulatory-compliant analytical characterization
Scalable production to support clinical trials
Custom formulation, stability, and compatibility testing
Process validation and GMP compliance for regulatory adherence