How to Deal with EU Medical Device New Barriers
Sep 26, 2013, 09:00
Sep 26, 2013, 17:00
Recent years, the scale of international medical device market expands rapidly and the needs for the medical device products also increase dramatically. The export of the medical device suffers from much more requirements from importing countries and clients. Foreign clients much concern about the quality of medical products, equipments and fittings, and request manufacturers and suppliers to provide best products.
With the strongest supporting ability, SGS invites you to participate in the seminar, provide the latest analysis on EU new regulations and share domestic and foreign cases to protect your exports.
Topic in the morning
Interpretation of revised EU medical device regulations
The new changes of medical device quality management standards made by the European Commission, and how to correspond and conform to the requirements of the new standards.
Topic in the afternoon
ISO 14971 Medical device risk management standard analysis
On the process of quality management, client service and product development, help medical device enterprises to forecast risks effectively and take control in efficient method.
- Contact Name: Ms Pang
- Contact Tel: 020-82075103