Grindeks AS
تقوم Grindeks AS بتصنيع المنتجات الصيدلانية لقنوات B2B الجاهزة للتصدير.
تقوم Grindeks AS بتصنيع المنتجات الصيدلانية والمكونات النشطة والأدوية الجاهزة في ريغا. تأسست الشركة في عام 1946، وتقوم بتزويد الصيدليات والمستشفيات وموزعي الرعاية الصحية وأسواق التصدير عبر LV وEE وLT وDE وأسواق التصدير ذات الصلة.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Riga, Latvia
- Founded
- 1946
- Website
- grindeks.com
- Categories
- اللوازم الطبية والرعاية الصحية
- Markets
- لاتفيا, إستونيا, ليتوانيا, ألمانيا
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
- domain-registered (green), checked 2026-08-02 Domain registry record
- gmp-certified (green), effective since 2026-03-03 EudraGMDP, EU register of GMP certificates (EMA)
- places-goods-on-market (green), checked 2026-08-07 Finnish Medicines Agency (Fimea), basic register of medicinal products
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- registry-active-global (green), checked 2026-07-07 Uzņēmumu reģistrs
- media-mention (green), checked 2026-07-18 Riga Stradiņš University
Profiles
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)