I have learnt that the accredited laboratories have regular Operational Staff Meetings (OSM) to discuss the correct interpretation of test standards and publish the draft/decision documents for compliance. When they conduct the verification testing according to the standards, they may or may not apply those decisions. What are the legal status of those decisions when we receive inquiry on test report submitted from market surveillances?
Is there any place to give the explanation/workflow of such OSM? Thanks and regards, Scott - ---------------------------------------------------------------- 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 <[email protected]> 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 <[email protected]> Mike Cantwell <[email protected]> For policy questions, send mail to: Jim Bacher: <[email protected]> David Heald: <[email protected]>
