Contipro a.s.
Productor checo de ácido hialurónico y fabricante por contrato para la industria farmacéutica y cosmética.
Contipro fabrica principios activos de ácido hialurónico, dispositivos médicos y activos cosméticos en Dolní Dobrouč. Fundada en 1991, la empresa suministra a formuladores farmacéuticos, fabricantes de dispositivos médicos y distribuidores de ingredientes cosméticos en todo el mundo.
- Type
- brand seeking distribution
- Location
- Dolní Dobrouč, Czechia
- Founded
- 1991
- Website
- contipro.com
- Categories
- Suministros médicos y sanitarios, Cuidado de la piel y cosmética
- Markets
- Chequia, Alemania, Estados Unidos, Japón
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 Aquí la adjudicación lleva además una comprobación ajena: en la UE y el EEE el comprador público debe excluir a los licitadores condenados por fraude, corrupción o blanqueo, y a aquellos con deudas tributarias o de cotizaciones establecidas por resolución firme. 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)