European rules for obtaining CE marking on products sold to EU Member States or in the EEA - conditions and product requirements for the conformity marking ...

A raft of new CE Marking Directives was implemented earlier in 2016. Amongst the nine new pieces of legislation was the third edition of the EMC Directive and new Low Voltage and ATEX Directives.

It is looking likely that RoHS will become a “CE Mark Directive” over the next couple of years. This could have a massive, resource sapping, impact on manufacturers, importers and distributors, ...

focused on understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing ...

The compliance process in electronics product development can appear intricate and precarious; especially so if mandatory rules or regulations are misinterpreted. Now, developers and OEMs have the ...

HUNTINGTON BEACH, Calif., Dec. 15, 2010 (GLOBE NEWSWIRE) -- iTech Medical, Inc. (OTCBB:IMSU) (Frankfurt:0IM), a medical information technology company, announced today that it has received CE Mark ...

MONTREAL, SoundBite Medical Solutions Inc. today announces it has received CE Marking for the SoundBite™ Crossing System, a unique and novel first-in-class wire-based technology that is intended for ...