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 ...

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, ...

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.

Module A from 768/2008 is the self-declaration procedure required for CE directives. This regulation affects the format of all new CE directives and so RoHS will be the first but it is likely that all ...

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 ...

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 ...

The European EMC Directive was fully implemented in the UK on 1 January 1996. Has it achieved what it set out to do? The short answer is ‘partially’. The EMC Directive is all about electrical ...