Lonza
البيولوجيا وواجهات برمجة التطبيقات ذات الجزيئات الصغيرة وتصنيع العلاج بالخلايا والجينات.
تقوم Lonza بتصنيع المواد البيولوجية وواجهات برمجة التطبيقات ذات الجزيئات الصغيرة وتصنيع العلاج بالخلايا والجينات من عملياتها في بازل. توفر الشركة أنظمة الرعاية الصحية والمختبرات وشركاء تصنيع المعدات الأصلية أو عملاء التصدير الخاضعين للتنظيم عبر أسواقها الرئيسية المدرجة.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Basel, Switzerland
- Founded
- 1897
- Website
- lonza.com
- Categories
- اللوازم الطبية والرعاية الصحية, المواد الكيميائية والبلاستيك
- Markets
- سويسرا, الولايات المتحدة, ألمانيا, سنغافورة
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
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- domain-registered (green), checked 2026-08-02 Domain registry record
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- operating-permit (green), checked 2026-09-16 SHAB, Swiss Official Gazette of Commerce
- lei-active (green), checked 2026-07-21 GLEIF
- sanctions-clear (green), checked 2026-07-21 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registry-active-global (green), checked 2026-07-21 Zefix (Swiss commercial registry)
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)