I keep on being told that when you manufacture medical devices in China ,for both the local market and the overseas market, that the registration and inspection requirements are much easier. Is this just wishful thinking or is it correct. In some ways I can see this being true for locally made devices sold in China but again, it is not clear to me.
Regards and thanks
Barry
EBR Consulting
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Barry Evers-Buckland
Director
Eltham North VIC
Australia
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