medicopack a , s
メディコパック
At MedicoPack, we develop and manufacture plastic packaging for pharmaceutical use within injection and infusion therapy for the global medical industry and hospitals. Design and development play an important role and through continuous optimisation and focus on innovation, we support safe use of medicine. Our packaging is manufactured under controlled conditions or in clean rooms that meet the ISO class 7 requirements. Quality Assurance is a high priority at MedicoPack. This is a prerequisite when manufacturing primary packaging that needs to meet the health authorities’ and the customers’ strict requirements to purity and quality.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Langeskov, Denmark
- Website
- https://www.medicopack.com
- Categories
- 医薬品製造, 包装および印刷用品
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- debarment-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
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