Servier
Formulaciones farmacéuticas, medicamentos genéricos y productos sanitarios.
Servier fabrica formulaciones farmacéuticas, medicamentos genéricos y productos sanitarios desde sus operaciones en Suresnes. La empresa abastece a canales de farmacias, compradores de hospitales, distribuidores de atención médica o clientes de exportación en sus mercados primarios listados.
- Type
- brand seeking distribution
- Location
- Suresnes, France
- Founded
- 1954
- Website
- servier.com
- Categories
- Suministros médicos y sanitarios, Suplementos y bienestar
- Markets
- Francia, Estados Unidos, Alemania, Brasil
Verified facts
- web-presence-since (green), checked 2026-08-20 Internet Archive (Wayback)
- facility-registered (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- domain-registered (green), checked 2026-08-26 Domain registry record
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- registry-active-global (green), checked 2026-08-30 INSEE Sirene (annuaire-entreprises)
- places-goods-on-market (green), checked 2026-08-30 Registre national des producteurs (ADEME/SYDEREP), France
- registered-since (green), checked 2026-08-30 INSEE Sirene (annuaire-entreprises)
- registry-id-verified (green), checked 2026-08-20 SIREN published in the company's own legal notice, confirmed in the French business register
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- 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)
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- media-mention (green), checked 2026-07-18 Kavout | AI
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- 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)