Medochemie Ltd
Cyprus's largest pharmaceutical company, exporting generic medicines to 122 countries.
Medochemie is the largest pharmaceutical manufacturer headquartered in Cyprus and one of the top 200 generics producers globally. The company operates 15 manufacturing facilities across Cyprus, the Netherlands, and Vietnam, producing 630 pharmaceutical products under more than 5,000 marketing authorisations and exporting to 122 countries.
- Type
- Manufacturer
- Location
- Limassol, Cyprus
- Founded
- 1976
- Website
- medochemie.com
- Categories
- Medical & Healthcare Supplies
- Markets
- Germany, Netherlands, Vietnam, United Kingdom, Greece
Verified facts
- product-authorised-for-sale (green), checked 2026-08-21 Ministry of Health of Armenia, State Register of Medicinal Products (pharm.am)
- 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
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- 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 2026-08-16 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 Here the award carries someone else's check: in the EU and the EEA a public buyer must exclude bidders convicted of fraud, corruption or money laundering, and those found by a final decision to owe taxes or social contributions. 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)