Janssen Pharmaceutica
ベルギーの医薬品製造
ヤンセン ファーマシューティカは、ベルギーのベールセに拠点を置く医薬品製造会社です。公的事業登録簿に登録されています。
- Type
- Manufacturer
- Location
- Beerse, Belgium
- Website
- https://janssen.com
- Categories
- 医薬品製造
Listed in a source registry
Verified facts
- market-access-eu (green), checked 2026-08-18 TRACES NT, European Commission register of approved establishments (DG SANTE)
- product-authorised-for-sale (green), checked 2026-08-20 NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- ownership-on-record (green), checked 2026-08-13 GLEIF global LEI index
- debarment-clear (green), checked 2026-08-14 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-14 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-14 OpenSanctions
- domain-registered (green), checked 2026-08-14 Domain registry record
- places-goods-on-market (green), checked 2026-08-16 Registre national des producteurs (ADEME/SYDEREP), France
- aeo-certified (green), checked 2026-08-16 EU AEO register (European Commission)
- registered-manufacturer (green), checked 2026-08-18 Chemistry, Food and Drugs Division, Ministry of Health of Trinidad and Tobago, register of drugs (Food and Drugs Act Chap. 30:01)
- operating-permit (green), checked 2026-08-08 EEA Industrial Emissions Portal (IED), EU-wide permit register
- lei-active (green), checked 2026-08-16 GLEIF global LEI register (golden copy)
- gmp-certified (green), checked 2024-03-26 EudraGMDP, EU register of GMP certificates (EMA)
- registry-id-verified (green), checked 2026-07-04 Crossroads Bank for Enterprises (KBO / BCE)
Claimed certifications
- Good Manufacturing Practice
- AEO, Authorised Economic Operator EU AEO database
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)