Rovi Pharma Industrial Services

ROISCDMO

Siamo conosciuti per la nostra competenza, dedizione costante e trasparenza nel campo della produzione conto terzi. Benvenuti a ROVI.

Type: brand seeking distribution
Location: Madrid, Spain
Website: https://www.roviservices.com
Categories: Produzione farmaceutica, Imballaggi e forniture per la stampa, Forniture medicali e sanitarie

Listed in a source registry

domain-registered (green), checked 2026-08-09 Domain registry record
sanctions-clear (green), checked 2026-08-09 OpenSanctions
corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
public-contract-awarded (green), checked 2026-05-13 TED (Tenders Electronic Daily), EU public procurement award notices 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)
facility-registered (green), checked 2026-08-30 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
debarment-clear (green), checked 2026-08-09 OpenSanctions
public-subsidy-received (green), checked 2026-08-16 BDNS, Base de Datos Nacional de Subvenciones (Ministerio de Hacienda)
vat-valid (green), checked 2026-08-16 VIES (European Commission)

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)
If the goods are paper, board or printed products, EU imports fall under the Deforestation Regulation (EUDR) due-diligence regime; packaging machinery itself does not. European Commission (EUDR)
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)
No public registry exists for certificates of this kind in this sector: conformity is declared by the manufacturer. European Commission: CE marking, manufacturer's conformity assessment