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For nearly 30 years we have helped the world’s most innovative bio/pharmaceutical companies to navigate the challenges of new product development, drug delivery, production, and market release. We provide a broad range of cGMP, GLP, GCP laboratory services, with a focus on support for the development and production of mRNA, oligos, peptides, biologics, or vaccines. We are adept in establishing GMP validated analytical methods including mRNA specific methods such as integrity, potency, capping efficiency, sequencing, Poly(A) Tail, residual DNA template, residual dsRNA and delivery system testing (e.g. lipid nanoparticles (LNPs)). These comprehensive characterisation services provide data to determine protein expression and product purity, which can be directly linked to translation efficiency and immunogenicity. We also provide ICH stability and formulation development programs and have leading expertise in the product development of inhaled and nasal drugs. Our outsourcing contracts are flexible and can be tailored to your specific timelines, requirements, and budgets.


Team Members

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Laura Nottle

Business Development Manager

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Cory Stoker

Associate Business Development Manager