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The Danish National Prescription Registry Request PDF
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How to notify the Product Registry - Arbejdstilsynet - at
WebOct 19, 2024 · The following entities must register with the DKMA if they are headquartered in Denmark: Manufacturers of medical devices in classes I, IIa, IIb and III, active implantable medical devices, custom made devices, and system and medical treatment packages (and Danish representatives of non-EU manufacturers), WebWho/what is the Product Register? The Product Register contains information on around 38,000 products on the market in Denmark and provides an overview which the Danish … WebSep 9, 2024 · Act No. 3 of 3 January 2024 – The Danish Product Safety Act Executive Orders and EU Commission Regulations The Ministry of Health's Executive Order No. 1263 of 15 December 2008 concerning medical devices The Ministry of the Interior and Health's Executive Order No. 1269 of 12 December 2005 concerning in vitro diagnostic medical … list of illicit opioids