Grindeks AS
Grindeks AS は、輸出対応の B2B チャネル向けの医薬品を製造しています。
Grindeks AS はリガで医薬品、有効成分、最終医薬品を製造しています。 1946 年に設立された同社は、薬局、病院、医療品販売業者、LV、EE、LT、DE および関連輸出市場の輸出市場に製品を供給しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Riga, Latvia
- Founded
- 1946
- Website
- grindeks.com
- Categories
- 医療およびヘルスケア用品
- Markets
- ラトビア, エストニア, リトアニア, ドイツ
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)