We’re nothing if not thorough

Our experience enables us to ask the right questions to get to the root of what our clients want to achieve, what problems they have identified and the solution they have developed to solve that problem.

Accredited to ISO 13485 (medical devices), ISO14001 (environmental) and ISO 9001 (electrical, electronic and mechanical assemblies), we use our experience to see beyond the challenges and support clients through each stage. We design and develop complex, innovative products and systems which require expert knowledge of relevant regulatory criteria. When vital decisions are made we make sure that every aspect of regulatory compliance, relevant to your product is understood. We guide clients through the regulatory requirements to future proof their route to market and to help navigate the challenges ahead.

We also work with organisations to help them gain ISO accreditation or set up their own regulatory systems. Contact us.

product design & development for:

Siemens gets CE-Mark for new diagnostic solution

Siemens Healthineers has received CE-Mark for its new Atellica Solution with immunoassay and chemistry analysers, which will allow commercial launch in Europe. The flexible, scalable, automation-ready in-vitro diagnostic (IVD) solution is designed to provide control and simplicity to diagnostic professionals,… more

Synaptive Medical introduces new surgical robotic device

Canadian firm Synaptive Medical has introduced its second-generation, high-powered Modus V digital microscope that has a robotic arm to aid neurosurgery. Modus V is based on Canadarm technology used at the International Space Station and is part of the firm’s… more