Contipro a.s.
İlaç ve kozmetik endüstrilerine yönelik Çek hyaluronik asit üreticisi ve fason üreticisi.
Contipro, Dolní Dobrouč'ta hyaluronik asit API'si, tıbbi cihazlar ve kozmetik aktif maddeler üretmektedir. 1991 yılında kurulan şirket, dünya çapında farmasötik formül hazırlayıcılara, tıbbi cihaz üreticilerine ve kozmetik içerik distribütörlerine tedarik sağlıyor.
- 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
- Tıbbi ve Sağlık Malzemeleri, Cilt Bakımı ve Kozmetik
- Markets
- Çekya, Almanya, Amerika Birleşik Devletleri, Japonya
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 Burada ihalenin kazanılması başkasının yaptığı bir denetimi de taşır: AB ve AEA'da kamu alıcısı, dolandırıcılık, yolsuzluk veya kara para aklamadan hüküm giymiş istekliler ile kesinleşmiş kararla vergi veya sosyal güvenlik borcu saptananları elemek zorundadır. 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)