Prasfarma
Startseite - Prasfarma
Entwicklung, Co-Entwicklung, Herstellung und Bereitstellung klinischer Chargen. Als Branchenführer haben wir uns der Spezialisierung in einem breiten Spektrum von Bereichen verschrieben. Entdecken Sie mehr Prasfarma, das Ihnen ein All-Inclusive-Angebot an pharmazeutischen Dienstleistungen zur Verfügung stellt. Mehr über uns, unsere Produkte, Know-how und Erfahrung in zytotoxischen und hochwirksamen Produkten. Entdecken Sie mehr zytostatische […]
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Spain
- Website
- https://prasfarma.com
- Categories
- Pharmazeutische Produktion
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
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- domain-registered (green), checked 2026-08-09 Domain registry record
- vat-valid (green), checked 2026-08-16 VIES (European Commission)
- public-subsidy-received (green), checked 2026-08-16 BDNS, Base de Datos Nacional de Subvenciones (Ministerio de Hacienda)
- 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)