Siegfried
医薬品有効成分と最終剤形。
ジークフリートは、ツォフィンゲンの事業で医薬品有効成分と最終剤形を製造しています。同社は、上場主要市場全体でヘルスケア システム、研究所、OEM パートナー、または規制対象の輸出顧客に供給しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Zofingen, Switzerland
- Founded
- 1873
- Website
- siegfried.ch
- Categories
- 医療およびヘルスケア用品, 化学薬品とプラスチック
- Markets
- スイス, ドイツ, アメリカ合衆国, 中国
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
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- registry-active-global (green), checked 2026-07-21 Zefix (Swiss commercial registry)
- sanctions-clear (green), checked 2026-07-21 OpenSanctions
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- 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)