fidia farmaceutici spa
イタリアの公式ウェブサイト - Fidia Farmaceutici S.P.A.
1946 年以来、Fidia Farmaceutici は医師、パートナー、患者に統合された効果的で安全な製品とサービスを提供するために研究開発に注力してきました。
- 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
- 医薬品製造, 包装および印刷用品, サプリメントとウェルネス
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 ここでの落札は、他者による審査も伴います。EUおよびEEAでは、公共調達者は詐欺、汚職、資金洗浄で有罪となった入札者、および確定した決定で税や社会保険料の未納が認定された入札者を排除しなければなりません。 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