bio_subbu
Super Moderator
TGA Guidelines on “Differences between the Australian and European Union medical device regulatory requirements” has been released as draft. This guidance document has been created to assist Australian manufacturers who export medical devices to the EU or who intend to export to the EU, Australian sponsors who wish to import CE marked medical devices into the Australian market & overseas manufacturers who wish to manufacture for both the European and Australian markets.
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NOTE: Dead Link Removed.
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