Third Expedited Approval Pathway Coming To China In January

China Food and Drug Administration is introducing a new priority-review designation pathway that many companies are expected to use, although it is not yet clear just how much time it will save compared with the standard approval process.

A third expedited approval procedure for medical devices will soon be available in China after regulators confirmed they would be introducing a priority-review designation pathway on Jan. 1, 2017.

The new priority-review and approval procedure is substantially the same as that which was proposed and issued for consultation in...

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