Our UKAS accredited and GMP licenced laboratories act as your extended QC team, delivering rapid, precise, and compliant testing to ensure product quality and release timelines are never compromised.

We validate the integrity and purity of your raw materials, providing the scientific evidence that manufacturers and regulators demand and forming a solid foundation for your R&D and manufacturing operations.

With in-process testing, we help you monitor, adjust, and optimise production in real-time minimising waste and ensuring process control.

Whether it’s tablets, capsules, aerolos, or innovative delivery formats, we ensure the final product meets all required specifications for efficacy and safety.

Our GMP qualified team provide efficient batch release testing and review ensuring your product gets to market quickly, with full compliance assurance.

We dive deep into understanding your product’s critical quality attributes, using cutting-edge analytical tools and methodologies to characterise even complex formulations.

Our ICH-compliant stability facility simulates real-world shelf-life scenarios helping you make evidence-based decisions about packaging, storage, and product expiration.

We design, refine, and validate analytical methods tailored to your product ensuring accuracy, precision, and repeatability under strict regulatory conditions like GMP.

We assess potential chemical interactions from container closure systems, helping you manage risk and comply with evolving regulatory demands.

Our development services support your product through every phase including pre-formulation, formulation, scale-up, and beyond.

We offer toxicological evaluations to determine safety thresholds for impurities, degradation products, and leachables that are essential for global health compliance.

Our team of regulatory experts align strategy with science to help you achieve successful approval outcomes.