Grindeks AS
Grindeks AS, ihracata hazır B2B kanalları için farmasötik ürünler üretmektedir.
Grindeks AS, Riga'da farmasötik ürünler, aktif maddeler ve bitmiş ilaçlar üretmektedir. 1946 yılında kurulan şirket, LV, EE, LT, DE ve ilgili ihracat pazarlarındaki eczanelere, hastanelere, sağlık distribütörlerine ve ihracat pazarlarına ürün tedarik etmektedir.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Riga, Latvia
- Founded
- 1946
- Website
- grindeks.com
- Categories
- Tıbbi ve Sağlık Malzemeleri
- Markets
- Letonya, Estonya, Litvanya, Almanya
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)