fidia farmaceutici spa

Sito Ufficiale Italia - Fidia Farmaceutici S.P.A.

Dal 1946 Fidia Farmaceutici è impegnata in ricerca e sviluppo, per offrire a medici, partner e pazienti prodotti e servizi integrati, efficaci e sicuri.

Type: manufacturer (our classification of the record, not a statement by the company)
Role: Manufacturer
Location: Abano Terme (PD), Italy
Founded: 1946
Website: https://www.fidiapharma.it
Categories: Produzione farmaceutica, Imballaggi e forniture per la stampa, Integratori e benessere

Listed in a source registry

CPHI exhibitor directory

What is established and what is not

No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.

Verified facts

operating-permit (green), effective since 2011-08-01 EEA Industrial Emissions Portal (IED), EU-wide permit register
registered-manufacturer (green), checked 2026-09-17 Ministero della Salute, banca dati e Repertorio dei dispositivi medici
public-contract-awarded (green), effective since 2026-07-13 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 2026-09-07 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
state-aid-sector (green), effective since 2026-06-03 Registro Nazionale degli Aiuti di Stato (rna.gov.it), open data
vat-valid (green), checked 2026-08-16 VIES (European Commission)
public-subsidy-received (green), checked 2026-08-25 OpenCoesione (opencoesione.gov.it), open data on project subjects

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

Full page for humans