Contipro a.s.
제약 및 화장품 산업을 위한 체코 히알루론산 생산자이자 계약 제조업체입니다.
Contipro는 Dolní Dobrouč에서 히알루론산 API, 의료 기기 및 화장품 활성 물질을 제조합니다. 1991년에 설립된 이 회사는 전 세계적으로 의약품 제조자, 의료 기기 제조업체 및 화장품 성분 유통업체에 제품을 공급하고 있습니다.
- 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
- 의료 및 건강 관리 용품, 스킨케어 및 화장품
- Markets
- 체코, 독일, 미국, 일본
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 여기서 낙찰은 남이 한 심사까지 함께 뜻합니다. EU와 EEA에서는 공공 발주자가 사기, 부패, 자금세탁으로 유죄가 확정된 입찰자와 최종 결정으로 세금 또는 사회보험료 체납이 확인된 입찰자를 반드시 배제해야 합니다. 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)