CIM A/S
Solutions logicielles validées GxP pour l’assemblage et le conditionnement pharmaceutique. Inspection visuelle, conformité numérique et
Solutions logicielles validées GxP pour l’assemblage et le conditionnement pharmaceutique. Inspection visuelle, conformité numérique et informations sur les données.
- Type
- brand seeking distribution
- Location
- Viby J, Denmark
- Founded
- 1998
- Website
- cim.as
- Categories
- Production pharmaceutique, Électronique grand public, Emballage et fournitures d'impression
Listed in a source registry
Verified facts
- domain-registered (green), checked 2026-07-28 Domain registry record
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
- export-registered (green), checked 2026-07-30 EU EORI validation (European Commission)
- annual-accounts-filed (green), checked 2026-08-16 Erhvervsstyrelsen, offentliggjorte årsrapporter (virk.dk)
Import rules for these goods
- If the goods are paper, board or printed products, EU imports fall under the Deforestation Regulation (EUDR) due-diligence regime; packaging machinery itself does not. European Commission (EUDR)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)
- No public registry exists for certificates of this kind in this sector: conformity is declared by the manufacturer. European Commission: CE marking, manufacturer's conformity assessment