Janssen Pharmaceutica
Sản xuất dược phẩm, Bỉ
Janssen Pharmaceutica là công ty sản xuất dược phẩm có trụ sở tại Beerse, Bỉ. Được liệt kê trong sổ đăng ký kinh doanh công cộng.
- Type
- Manufacturer
- Location
- Beerse, Belgium
- Website
- https://janssen.com
- Categories
- Sản xuất dược phẩm
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)