Grindeks AS
ग्रिंडेक्स एएस निर्यात के लिए तैयार बी2बी चैनलों के लिए फार्मास्युटिकल उत्पाद बनाती है।
ग्रिंडेक्स एएस रीगा में फार्मास्युटिकल उत्पाद, सक्रिय सामग्री और तैयार दवाएं बनाती है। 1946 में स्थापित, कंपनी एलवी, ईई, एलटी, डीई और संबंधित निर्यात बाजारों में फार्मेसियों, अस्पतालों, स्वास्थ्य सेवा वितरकों और निर्यात बाजारों को आपूर्ति करती है।
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Riga, Latvia
- Founded
- 1946
- Website
- grindeks.com
- Categories
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ
- Markets
- लातविया, एस्टोनिया, लिथुआनिया, जर्मनी
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)