BIA SEPARATIONS Podjetje za separacijske tehnologije d.o.o.
Словенский промышленный производитель и экспортер
BIA SEPARATIONS Podjetje za separacijske tehnologije d.o.o. зарегистрирована Sloexport в химическом и фармацевтическом секторе. В его каталоге описаны операции, в том числе компания BIA Separations Ltd., расположенная в Айдовщине, Словения, была основана группой ученых и венчурных инвесторов с целью разработки инновационных хроматографических материалов для следующего столетия и миссии стать лидером рынка в так называемых монолитных технологиях. Сегодня производитель BIA Separations.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ajdovščina, Slovenia
- Website
- https://biaseparations.com
- Categories
- Фармацевтическое производство, Медицинские товары и расходники, Химия и пластмассы
- Markets
- Словения, Австрия, Германия, Италия, Хорватия
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
- corporate-mail-on-domain (green), checked 2026-08-05 Mail server of the company domain
- domain-registered (green), checked 2026-08-05 Domain registry record
- web-presence-since (green), checked 2026-08-05 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
Import rules for these goods
- Chemical substances imported into the EU above 1 tonne/year must be REACH-registered. ECHA (REACH)
- 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)