Effective January 24, 2013, the European Union will require products placed on the market to comply with EN 60950-1:2006/ A11:2009/ A12:2011 and effective March 1, 2013, A1:2010 will also be... read more →
On August 5, 2013, the U.S. FDA announced the extension of the transition date for IEC 60601-1 3rd edition from June 30, 2013 to December 31, 2013. This means FDA... read more →
Taiwan BSMI published a new draft Standard on 26th of July 2013. The publish draft number is 10230015100. The draft is a new regulation for secondary lithium cells /cells pack、secondary... read more →
There were three major changes to South Korea’s Medical Devices Act and the Enforcement of the Medical Devices Act as of May 8th, 2013. 1. Introduction of IEC 60601-1 (third... read more →