CIM A/S
GxP-validated software solutions for pharma assembly and packaging. Vision inspection, digital compliance and data insights
GxP-validated software solutions for pharma assembly and packaging. Vision inspection, digital compliance and data insights.
- Type
- Manufacturer
- Location
- Viby J, Denmark
- Founded
- 1998
- Website
- cim.as
- Categories
- Pharmaceutical Manufacturing, Consumer Electronics, Packaging & Printing Supplies
Listed in a source registry
Verified facts
- domain-registered (green), checked 2026-07-28 Domain registry record
- export-registered (green), checked 2026-07-30 EU EORI validation (European Commission)
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
- annual-accounts-filed (green), checked 2026-08-16 Erhvervsstyrelsen, offentliggjorte årsrapporter (virk.dk)
Import rules for these goods
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)
- 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