May employees of companies making, importing or distributing medical devices be present in the surgical area? Yes, but only under certain conditions.
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The European Commission is looking for experts for panels on medical devices and in-vitro diagnostics
Later this year, the European Commission will launch a call for experts in medical devices and devices for in-vitro diagnostics. They will form expert panels to provide advice and assess new risky devices.
Recognition of the FAMHP by the American Food and Drug Administration (FDA)
The American Food and Drug Administration (FDA) has recognised the FAMHP as its Belgian counterpart under the mutual recognition agreement (MRA) between the European Union and the United States.
Second recast symposium – 13th June 2017
Following the success of the first session of the recast symposium, the FAMHP organises, as the competent authority, on Tuesday 13th June 2017 a second session of this symposium over the latest official information about the recast.