Contipro a.s.
Produsen asam hialuronat Ceko dan produsen kontrak untuk industri farmasi dan kosmetik.
Contipro memproduksi API asam hialuronat, peralatan medis, dan bahan aktif kosmetik di Dolní Dobrouč. Didirikan pada tahun 1991, perusahaan ini memasok formulasi farmasi, produsen perangkat medis, dan distributor bahan kosmetik di seluruh dunia.
- 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
- Perlengkapan Medis & Kesehatan, Perawatan Kulit & Kosmetik
- Markets
- Ceko, Jerman, Amerika Serikat, Jepang
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 Di sini kemenangan tender juga membawa pemeriksaan pihak lain: di UE dan EEA, pembeli publik wajib menggugurkan peserta yang dipidana karena penipuan, korupsi, atau pencucian uang, serta yang tunggakan pajak atau iurannya ditetapkan lewat putusan final. 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)