Prasfarma
Beranda - Prasfarma
Pengembangan, pengembangan bersama, manufaktur, dan pasokan batch klinis Sebagai pemimpin dalam industri, kami telah mendedikasikan diri untuk menawarkan spesialisasi di berbagai bidang. Temukan lebih banyak tempat Prasfarma yang dapat Anda gunakan dengan penawaran layanan farmasi yang lengkap. Lebih Banyak Tentang Kami produk kami Pengetahuan dan Pengalaman dalam Produk Sitotoksik dan Potensi Tinggi Temukan lebih banyak Sitostatika […]
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Spain
- Website
- https://prasfarma.com
- Categories
- Manufaktur Farmasi
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)