18 April 2013 – The NB-MED EN62304:2006 issues team released their first official version (V1.0) dated 5 April 2013 of this importnat implementation document in regards to EN 62304 with respect to the Medical Device Directive 93/42/EEC on the NB-MED website. EN
Date Change for Presentation on IEC60601-1, 3rd edition, Amendment 1 and its Impact on Users
NOTE: The previous posting and Events webpage was April 18, 2013 for the date of this presentation. FX Conferences had to change the date of the presentation for unforeseen circumstances and so it now will be on May 2, 2013 (Thurs)
Presentation on IEC60601-1, 3rd edition, Amendment 1 and its Impact on Users
Leo Eisner will be speaking on “IEC 60601–1, 3rd Edition, Amendment 1 and its Impact on Users” at an FX Conferences event on May 2, 2013 (Thurs) at 11:00AM – Noon (Pacific), 2:00PM – 3:00PM (Eastern). You don’t have to
Which 60601-1, 3rd ed. Standard Applicable for FDA?
I have been asked in a variety of flavors if 3rd ed. of IEC 60601-1:2005 and/or 3rd ed. + Amendment 1 (A1):2012 will be required by the FDA and when? The answer isn’t exactly yes or no. The end of
Proposal for FDA Create New Office to Regulate Mobile Apps
11 Feb 2013 – Regulatory Focus (RAPS) News Article indicates that there will be a re-introduced proposal going thru the US Congress, sometime this year, for the FDA’s CDRH to create a new office to Regulate Mobile Medical Device Applications. What