EN ISO 12100 is good and useful but EN ISO 14971 "Medical devices — Application of risk management to medical devices” is actually more relevant to some consumer type products
Nick. > On 31 Mar 2016, at 20:32, Nyffenegger, Dave <dave.nyffeneg...@bhemail.com> > wrote: > > Risk assessments are not new and it’s a requirement of the current Machinery > Directive from 2006 and probably for some time before. A principle HS for > the MD is EN ISO 12100:2010. Many of the basic concepts can be applied to > non-machinery. I’d think that standard or one similar would become an HS for > the LVD. > - ---------------------------------------------------------------- This message is from the IEEE Product Safety Engineering Society emc-pstc discussion list. To post a message to the list, send your e-mail to <emc-p...@ieee.org> All emc-pstc postings are archived and searchable on the web at: http://www.ieee-pses.org/emc-pstc.html Attachments are not permitted but the IEEE PSES Online Communities site at http://product-compliance.oc.ieee.org/ can be used for graphics (in well-used formats), large files, etc. Website: http://www.ieee-pses.org/ Instructions: http://www.ieee-pses.org/list.html (including how to unsubscribe) List rules: http://www.ieee-pses.org/listrules.html For help, send mail to the list administrators: Scott Douglas <sdoug...@ieee.org> Mike Cantwell <mcantw...@ieee.org> For policy questions, send mail to: Jim Bacher: <j.bac...@ieee.org> David Heald: <dhe...@gmail.com>
