Blog contribution by Edgar Kasteel. Companies wanting to sell their devices in Europe should consider not only where they want to sell, but what they need to accomplish. Loading up a crate of goods, calling UPS and crossing fingers do not make a viable business plan.
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On the back of the World Economic Forum, Swiss Federal Councillor Alain Berset and Zhang Yong, the minister responsible for the China Food and Drug Administration (CFDA), signed a bilateral agreement relating to medical devices on 21 January 2015.
……and should solve major quality and safety issues. Every time there is a public health scandal of some substance, the authorities respond with an overhaul of the relevant regulations. This was the case after the PIP (Poly Implant Prothèse) breast implant scandal.