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:

The 10 largest medical device companies in the world

Mergers & acquisitions continue to change the medical device landscape, as reflected in Medical Design & Outsourcing’s new Big 100 list. We pulled financial regulatory filings and reached out to major companies in some cases to create a list of… more

Triteq will be exhibiting at the Innovation for Leaders Conference on the 4th and 5th December

Triteq are exhibiting at the Innovation Forum 2017 Leaders Conference. The Innovation Forum – Leaders Conference is a C-level conference gathering top leaders from industry, academia and government and mixing them with early-stage ventures investors and researchers. The conference is… more