Bioveta, a.s.
Fabrication pharmaceutique, Tchéquie
Bioveta, a.s. est une entreprise de fabrication pharmaceutique basée à Ivanovice Na Hané, en Tchéquie. Inscrite au registre public des entreprises.
- Type
- Manufacturer
- Location
- Ivanovice Na Hané, Czechia
- Founded
- 1996
- Categories
- Production pharmaceutique
Listed in a source registry
Verified facts
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- places-goods-on-market (green), checked 2026-08-07 Finnish Medicines Agency (Fimea), basic register of medicinal products
- registry-active-global (green), checked 2026-08-24 ARES (Czech business register)
- registered-since (green), checked 1996-07-01 ARES (Czech business register)
- registered-manufacturer (green), checked 1996-07-01 ARES (Czech business register)
- directors-on-file (green), checked 2026-08-24 ARES (Czech business register)
- leadership-on-record (green), checked 2023-07-11 ARES (Czech business register)
- public-contract-awarded (green), checked 2026-06-02 TED (Tenders Electronic Daily), EU public procurement award notices Ici l'attribution porte aussi un contrôle fait par d'autres: dans l'UE et l'EEE, l'acheteur public doit exclure les candidats condamnés pour fraude, corruption ou blanchiment, ainsi que ceux dont une décision définitive a établi des dettes fiscales ou sociales. Directive 2014/24/EU, Article 57 (exclusion grounds)
- operating-permit (green), checked 2026-08-16 EudraGMDP manufacturing authorisation register (EMA)
- gmp-certified (green), checked 2025-03-14 EudraGMDP, EU register of GMP certificates (EMA)
- export-registered (green), checked 2026-08-12 EU EORI validation (European Commission)
- vat-valid (green), checked 2026-08-08 VIES (European Commission)
- workforce-on-record (green), checked 2026-08-16 ARES, registr ekonomických subjektů (Česká republika)
Claimed certifications
- Good Manufacturing Practice
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)