fidia farmaceutici spa

Listed in a source registry

CPHI exhibitor directory

Verified facts

• registered-manufacturer (green), checked 2026-08-22 OpenCoesione (opencoesione.gov.it), open data on project subjects
• state-aid-sector (green), checked 2026-06-03 Registro Nazionale degli Aiuti di Stato (rna.gov.it), open data
• operating-permit (green), checked 2011-08-01 EEA Industrial Emissions Portal (IED), EU-wide permit register
• public-contract-awarded (green), checked 2026-07-13 TED (Tenders Electronic Daily), EU public procurement award notices 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)
• facility-registered (green), checked 2026-08-16 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
• vat-valid (green), checked 2026-08-16 VIES (European Commission)

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)
• 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

Check independently

• Sanctions and watchlists (OpenSanctions)
• VAT number check (EU VIES)