Ofichem
Uzman İlaç CDMO Hizmetleri | Ofichem
Ofichem, tam GMP uyumluluğu kapsamında yüksek kaliteli ilaç maddesi ve ilaç ürünü geliştirme, üretim ve düzenleyici destek sağlayan güvenilir bir CDMO'dur.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Netherlands
- Founded
- 1975
- Website
- https://ofichem.com
- Categories
- İlaç Üretimi
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
- domain-registered (green), checked 2026-08-09 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Import rules for these goods
- 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)