A European Commission report released Wednesday predicts a majority of medical devices and drugs will be compliant with EU legislation ahead of Brexit, which has been delayed until Oct. 31. The EC also noted that "in duly justified cases" for certain medical devices and in-vitro diagnostics, member states may be able "to authorise UK certificate holders to continue placing their products on the market in the territory of the Member State concerned for a limited period of time."
EC report: Most medical products should be compliant before Brexit
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