CE marking your product?

06 October 2017

Get a free consultation with Medilink member Triteq

At triteq, we don’t just tick the boxes because we have to. When it comes to regulatory and standards, triteq will work with you throughout your entire design process and advise you on the best route for getting your product CE marked. 

We 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 how to make products happen ensures we support our clients from innovation to market, concept to product and service to adoption. New requirements for ISO14001, ISO9001 and ISO13485 come into effect September 2018. Triteq already has all the new documentation in place for all of these changes and we are engaging with BSI on an audit schedule to verify these requirements. The changes place greater emphasis on risks and opportunities for companies.

Find out more about standards and accreditation. 

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