Contipro a.s.
Czeski producent kwasu hialuronowego i producent kontraktowy dla przemysłu farmaceutycznego i kosmetycznego.
Contipro produkuje kwas hialuronowy API, wyroby medyczne i aktywne kosmetyki w Dolním Dobrouču. Założona w 1991 roku firma zaopatruje formulatorów farmaceutycznych, producentów wyrobów medycznych i dystrybutorów składników kosmetyków na całym świecie.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Dolní Dobrouč, Czechia
- Founded
- 1991
- Website
- contipro.com
- Categories
- Artykuły medyczne i związane z opieką zdrowotną, Pielęgnacja skóry i kosmetyki
- Markets
- Czechy, Niemcy, Stany Zjednoczone, Japonia
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
- 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)
- gmp-certified (green), effective since 2025-12-09 EudraGMDP, EU register of GMP certificates (EMA)
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- registered-since (green), effective since 1994-12-30 ARES (Czech business register)
- directors-on-file (green), checked 2026-09-17 ARES (Czech business register)
- leadership-on-record (green), effective since 2014-11-19 ARES (Czech business register)
- public-contract-awarded (green), effective since 2024-08-30 TED (Tenders Electronic Daily), EU public procurement award notices Tutaj wygrana niesie też cudzą kontrolę: w UE i EOG zamawiający musi wykluczyć wykonawcę skazanego za oszustwo, korupcję lub pranie pieniędzy oraz takiego, wobec którego prawomocnie stwierdzono zaległości podatkowe lub składkowe. Directive 2014/24/EU, Article 57 (exclusion grounds)
- 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
- facility-registered (green), checked 2026-09-07 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
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)