Contipro a.s.
Producteur tchèque d'acide hyaluronique et fabricant sous contrat pour les industries pharmaceutique et cosmétique.
Contipro fabrique de l'acide hyaluronique API, des dispositifs médicaux et des actifs cosmétiques à Dolní Dobrouč. Fondée en 1991, la société fournit des formulateurs pharmaceutiques, des fabricants de dispositifs médicaux et des distributeurs d'ingrédients cosmétiques dans le monde entier.
- Type
- brand seeking distribution
- Location
- Dolní Dobrouč, Czechia
- Founded
- 1991
- Website
- contipro.com
- Categories
- Fournitures médicales et de santé, Soins et cosmétiques
- Markets
- Tchéquie, Allemagne, États-Unis, Japon
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- market-access-eu (green), checked 2026-08-22 TRACES NT, European Commission register of approved establishments (DG SANTE)
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- registered-since (green), checked 1994-12-30 ARES (Czech business register)
- gmp-certified (green), checked 2025-12-09 EudraGMDP, EU register of GMP certificates (EMA)
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- directors-on-file (green), checked 2026-08-24 ARES (Czech business register)
- leadership-on-record (green), checked 2014-11-19 ARES (Czech business register)
- public-contract-awarded (green), checked 2024-08-30 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)
- facility-registered (green), checked 2026-08-30 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- export-registered (green), checked 2026-07-30 EU EORI validation (European Commission)
- registry-activity (green), checked 2026-07-08 ARES
- registry-active-global (green), checked 2026-07-08 ARES
- media-mention (green), checked 2026-07-18 Happi | Household And Personal Products Industry
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- Good Manufacturing Practice
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)