Grindeks AS
Grindeks AS는 수출용 B2B 채널용 의약품을 제조합니다.
Grindeks AS는 리가에서 의약품, 활성 성분 및 완제품을 제조합니다. 1946년에 설립된 이 회사는 LV, EE, LT, DE 및 관련 수출 시장 전반에 걸쳐 약국, 병원, 의료 유통업체 및 수출 시장에 제품을 공급합니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Riga, Latvia
- Founded
- 1946
- Website
- grindeks.com
- Categories
- 의료 및 건강 관리 용품
- Markets
- 라트비아, 에스토니아, 리투아니아, 독일
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)