TÜV SÜD China will host Seminar "Affects of the latest European Union Medical Device Directive"
01.03.2010
Introduction:
New MDD 2007/47/EC was issued on 2 Sep, 2007, which revised the Device Directive (93/42/EEC), Active Implantable Medical Device Directive and Biocidal Products Directive (98/8/EC). The latest Directive will constrain to the manufactures from Mar, 21, 2010.
Technical Newsletter
03.02.2012
New PAH requirements for GS Mark
New PAH requirements for GS Mark
03.02.2012
Harmonization of safety requirements for batteries
Harmonization of safety requirements for batteries
03.02.2012
TÜV SÜD becomes an officially recognized certification body for NRCan
TÜV SÜD becomes an officially recognized certification body for NRCan
17.01.2012
TÜV SÜD Energy Mark
TÜV SÜD Energy Mark