Medochemie Ltd
La più grande azienda farmaceutica di Cipro, che esporta medicinali generici in 122 paesi.
Medochemie è il più grande produttore farmaceutico con sede a Cipro e uno dei primi 200 produttori di farmaci generici a livello globale. L'azienda gestisce 15 stabilimenti produttivi tra Cipro, Paesi Bassi e Vietnam, producendo 630 prodotti farmaceutici con oltre 5.000 autorizzazioni all'immissione in commercio ed esportando in 122 paesi.
- Type
- brand seeking distribution
- Location
- Limassol, Cyprus
- Founded
- 1976
- Website
- medochemie.com
- Categories
- Forniture medicali e sanitarie
- Markets
- Germania, Paesi Bassi, Vietnam, Regno Unito, Grecia
Verified facts
- product-authorised-for-sale (green), checked 2026-08-21 Ministry of Health of Armenia, State Register of Medicinal Products (pharm.am)
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-12 OpenSanctions
- sanctions-clear (green), checked 2026-08-12 OpenSanctions
- domain-registered (green), checked 2026-08-12 Domain registry record
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- public-contract-awarded (green), checked 2026-07-31 Treasury of the Republic of Cyprus, eProcurement register of awarded public contracts, via data.gov.cy Qui l'aggiudicazione porta con sé anche un controllo altrui: nell'UE e nello SEE la stazione appaltante deve escludere gli operatori condannati per frode, corruzione o riciclaggio e quelli con debiti fiscali o contributivi accertati con decisione definitiva. Directive 2014/24/EU, Article 57 (exclusion grounds)
- directors-on-file (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
- leadership-on-record (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
- registered-address (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
- registered-since (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
- registry-active-global (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
- registry-id-verified (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- Good Manufacturing Practice
- CE Marking EU NANDO (notified bodies)
- AEO, Authorised Economic Operator EU AEO database
Import rules for these goods
- 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)