Rottendorf Pharma GmbH
Rottendorf Pharma GmbH は、製薬業界に重点を置いた世界有数の受託開発製造組織 (CDMO) です。 1928年に設立されたロッテンドルフ…
Rottendorf Pharma GmbH は、製薬業界に重点を置いた世界有数の受託開発製造組織 (CDMO) です。 1928年に設立されたロッテンドルフ…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Germany
- Founded
- 1928
- Website
- http://rottendorf.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
- product-authorised-for-sale (green), checked 2026-08-20 NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- gmp-certified (green), effective since 2024-03-14 EudraGMDP, EU register of GMP certificates (EMA)
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- vat-valid (green), checked 2026-08-22 VIES (European Commission)
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- 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)
- registry-active-global (green), checked 2026-07-08 Handelsregister (North Data)
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)