Medical Device Design Obsolescence: Upgrade or Redesign?
How do you manage obsolescence in medical device designs – upgrade or redesign? Read our new guide for key product design issues to consider…
UKCA and CE marking – what you need to know
UKCA and CE Marking – Your Questions Answered Within the EU, CE marking is mandatory for machinery, electrical and electronic equipment, medical devices, personal protective equipment and toys. As such, anyone looking to sell electrical products in the EU will need to test for compliance and affix a CE mark to their product. Post Brexit, […]
Radio Equipment Directive – what you need to know in 2019
Radio Equipment Directive – What You Need to Know in 2019 As electronics product designers we know that the compliance process in electronics product development can appear intricate and precarious, if rules or regulations are misinterpreted. Now, our community has the European Union’s new Radio Equipment Directive 2014/53/EU (RED) to grapple with. The RED was […]
CE marking – 20 things you need to know
CE marking – 20 things you need to know Placed on several categories of products, CE marking is mandatory for machinery, electrical and electronic equipment, medical devices, personal protective equipment and toys. We recently published updated advice for CE and UKCA marking to get you up to date on how compliance law is changing and […]