Solupharm Pharmazeutische Erzeugnisse GmbH
Solupharm Pharmazeutische Erzeugnisse GmbH は、製薬業界の著名なサプライヤーであり、製薬業界のさまざまなニーズに応える包括的なサービスの提供を専門としています。
Solupharm Pharmazeutische Erzeugnisse GmbH は、製薬業界の著名なサプライヤーであり、製薬業界のさまざまなニーズに応える包括的なサービスの提供を専門としています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Germany
- Founded
- 1974
- Website
- http://solupharm.com
- Categories
- 医薬品製造
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
- domain-registered (green), checked 2026-08-02 Domain registry record
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
- registered-manufacturer (green), checked 2026-08-21 Jordan Food and Drug Administration (JFDA), approved manufacturing sites (open data portal of Jordan)
- product-authorised-for-sale (green), checked 2026-08-21 Ministry of Health of Armenia, State Register of Medicinal Products (pharm.am)
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- gmp-certified (green), effective since 2025-06-27 EudraGMDP, EU register of GMP certificates (EMA)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Profiles
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)