We support Chemistry, Manufacturing & Controls (CMC) activities to ensure your drug product meets quality, safety and regulatory standards. From early-phase development through to tech transfer, our consultants bring cross-functional expertise in chemistry, manufacturing and regulatory alignment.

Our formulation experts help you develop and optimise drug delivery systems, ensuring stability, bioavailability and patient compliance. We support both small molecule and biologic formulations across a range of dosage forms.

We assist in designing, validating and executing robust analytical methods to characterise drug substances and products. Our consultants help ensure regulatory compliance and analytical accuracy across the full development cycle.

We support medical device companies in R&D, from concept and prototyping to design verification and usability testing. Our expertise covers software and hardware development, risk management and regulatory design controls (ISO 13485, MDR).

We offer support in data-driven research, helping you extract insights from genomic, proteomic and other biological datasets. Our bioinformaticians bridge the gap between biology and data science to accelerate discovery and development.

Our consultants support R&D in biobased materials, functional coatings, green solvents and other innovative solutions. We work across lab, pilot and scale-up environments to enable sustainable material breakthroughs.

From lab-scale feasibility to pilot and industrial implementation, we help optimise chemical and biotechnological processes. Our engineers and scientists focus on efficiency, safety and scalability, aligned with sustainability goals.