Biotika a.s.
Biotika a.s. produkuje substancje farmaceutyczne dla gotowych do eksportu kanałów B2B.
Biotika a.s. produkuje substancje farmaceutyczne, antybiotyki, produkty weterynaryjne i leki w Slovenska Lupca. Założona w 1953 roku firma zaopatruje dystrybutorów farmaceutycznych, szpitale, kanały weterynaryjne i odbiorców eksportowych w SK, CZ, DE, PL i powiązanych rynkach eksportowych.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Slovenska Lupca, Slovakia
- Founded
- 1953
- Website
- biotika.sk
- Categories
- Artykuły medyczne i związane z opieką zdrowotną
- Markets
- Słowacja, Czechy, Niemcy, Polska
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
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- registry-activity (green), checked 2026-08-21 Enviroportál SAŽP, centrálny informačný systém EIA/SEA (environmental impact assessment, Slovakia)
- operating-permit (green), checked 2026-08-16 EudraGMDP manufacturing authorisation register (EMA)
- corporate-mail-on-domain (green), checked 2026-08-06 Mail server of the company domain
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- sanctions-clear (green), checked 2026-08-06 OpenSanctions
- debarment-clear (green), checked 2026-08-06 OpenSanctions
- gmp-certified (green), effective since 2025-12-11 EudraGMDP, EU register of GMP certificates (EMA)
- facility-registered (green), checked 2026-09-07 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)