Seminar on EU and US Regulations Trends for Medical Devices and IEC60601 New Interpretation
Jun 14, 2013, 14:00
Jun 14, 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.
- Passive medical devices
- EU Medical Devices New Order
- US FDA Requirements
Contact: Ms. Pang