Laboratorios Rovi
Formulaciones farmacéuticas, medicamentos genéricos y productos sanitarios.
Laboratorios Rovi fabrica formulaciones farmacéuticas, medicamentos genéricos y productos sanitarios desde sus operaciones en Madrid. La empresa abastece a canales de farmacias, compradores de hospitales, distribuidores de atención médica o clientes de exportación en sus mercados primarios listados.
- Type
- Manufacturer
- Location
- Madrid, Spain
- Founded
- 1946
- Website
- rovi.es
- Categories
- Suministros médicos y sanitarios, Suplementos y bienestar
- Markets
- España, Estados Unidos, Alemania, Francia
Verified facts
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- lei-active (green), checked 2026-08-09 GLEIF
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- product-authorised-for-sale (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- vat-valid (green), checked 2026-08-09 VIES
- public-contract-awarded (green), checked 2026-05-13 TED (Tenders Electronic Daily), EU public procurement award notices Aquí la adjudicación lleva además una comprobación ajena: en la UE y el EEE el comprador público debe excluir a los licitadores condenados por fraude, corrupción o blanqueo, y a aquellos con deudas tributarias o de cotizaciones establecidas por resolución firme. Directive 2014/24/EU, Article 57 (exclusion grounds)
- export-registered (green), checked 2026-08-09 EU EORI validation (European Commission)
- public-subsidy-received (green), checked 2026-08-16 BDNS, Base de Datos Nacional de Subvenciones (Ministerio de Hacienda)
Profiles
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)