We frequently design and develop complex, innovative products and systems which require expert knowledge of relevant regulatory criteria. When vital decisions need to be made we make sure that every aspect of regulatory compliance, relevant to your product is understood.
We carry out conformity assessments and manage the process for all aspects of CE Marking, ATEX and safety critical medical device approval. Our accumulated experience of making products happen ensures we support our clients from innovation to market, concept to product and service to adoption.
As a multi-disciplinary product design consultancy we go beyond the standard route.Bringing real experience and industry knowledge to our clients ideas ensures smarter and faster results, with no compromise on regulatory compliance and commercial understanding. We are accredited to ISO 13485, 9001, 14001 through BSI.
Triteq have always focused on creating the right balance between innovative product design and regulatory compliance and have an excellent track record for helping our clients achieve objectives on time and in budget.
We provide informed regulatory advice and practical guidance on regulatory compliance, this can be a straightforward process, provided you have the right advice and work closely with an experienced product design and regulatory consultancy. It is our responsibility to guide clients through the regulatory requirements to future proof their route to market and to help navigate the challenges ahead.