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Introduction to FAMHP portal – manufacturing inspections
Belgium The FAMHP will open a new web portal later this year for manufacturers based in Belgium who are subject to inspections in the context of a GMP certificate, manufacturing and import authorization (MIA), raw materials (AR 97), active ingredients (API) or...
RD export 19/01/2023 – mandatory application for export
Belgium The Belgian government has issued a royal decree (19 January 2023) allowing the export of medicines to be temporarily restricted. The decree allows an export in case of unavailability to be subject to prior authorisation, if it concerns essential medicines and...
Fiscal importation of medicines from 3rd countries
Belgium The FAMHP again confirms and clarifies their interpretation of the rules set out in Annex 21 in the light of fiscal importation of medicines: “Fiscal importation” means the purchase/procurement 'on paper' of medicines that have not left the territory of the...
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