Claranor SA
Claranor는 펄스광 및 UV 기술을 사용하여 유제품, 음료, 식품, 그리고 최근에는 제약 및 화장품 산업을 위한 포장 살균 솔루션을 개발합니다. 장비
Claranor는 펄스광 및 UV 기술을 사용하여 유제품, 음료, 식품, 그리고 최근에는 제약 및 화장품 산업을 위한 포장 살균 솔루션을 개발합니다. 장비
- Type
- brand seeking distribution
- Location
- Avignon, France
- Website
- claranor.com
- Categories
- 의약품 제조, 유제품, 음료수
Listed in a source registry
Verified facts
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- workforce-on-record (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- facility-registered (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- domain-registered (green), checked 2026-08-26 Domain registry record
- lei-lapsed (amber), checked 2026-08-23 GLEIF global LEI register (golden copy)
- financials-published (green), checked 2020-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- listed-in-registry (green), checked 2026-08-26 BRIS, EU business registers interconnection (e-justice.europa.eu)
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- registry-id-verified (green), checked 2026-08-20 SIREN published in the company's own legal notice, confirmed in the French business register
- registry-active-global (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
- registry-activity (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)