TÜV SÜD China North Region will hold the three day seminar in Tianjin from Apr. 23th to 25th , which will include the latest CE Medical directive, risk management ISO 14971 of medical device products, RTTE1999/5/EC.
On March 21, 2010, the EC Directive 2007/47/EC has already become effective. This Directive will have a big impact on the Directives 93/42/EEC. Every manufacturer declaring conformity of his products to either of these EC Directives should be aware of that all medical devices according to 93/42/EEC must also comply with the new EC Directive from March 21, 2010 on – otherwise the products cannot be placed on the European market.
Impact on the following item ：
Classification of medical devices
Declaration of Conformity
2. Who should attend?
The relevant people from Medical devices manufactures, quality supervisor, R&D, Testing engineers, QC, QA and other people who show interests in Medical devices regulation.
3. Training Fee
￥ 3000/Person (Incl. Training, Dinner)
￥3500 /Person (Incl. Twin room, Training, Dinner)
￥4000 /Person (Incl. Single room, Training, Dinner)
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