fidia farmaceutici spa
Sito Ufficiale 意大利 - Fidia Farmaceutici S.P.A.
自 1946 年以来，Fidia Farmaceutici 一直致力于研发，为医生、合作伙伴和患者提供一体化、有效和安全的产品和服务。
- 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
- 药品制造, 包装及印刷用品, 补充剂与健康
Listed in a source registry
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 在这里，中标还附带了别人做过的审查：在欧盟和欧洲经济区，公共采购方必须排除因欺诈、腐败或洗钱被定罪的投标人，以及经终局裁决认定拖欠税款或社会保险费的投标人。 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