Total 26
No Subject Name Date Hit
11 CE Mark Approcal Process for medical Devices CE Manager 10-14 442
10 What is the role of an EU Authorized Representative? CE Manager 10-02 379
9 European Countries That Require CE Marking CE Manager 09-20 382
8 New Directive 2009/48/EC on toy safety CE Manager 09-10 350
7 CE_Content of Technical Files for Medical Devices CE Manager 09-08 358
6 LABEL_ MDD 2007/47/EC CE Manager 09-01 366
5 The definition of "electrical equipment' and the Equipm… CE Manager 08-23 362
4 SSSDSD SDSA 08-23 369
3 MDD 2007/47/EC revision contents summary CE Manager 08-13 379
2 CE MDD 93/42/EEC as amended by MDD 2007/47/EC CE Manager 07-30 387
1 GMP/GIP Guideline of KFDA Manager 03-20 793
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