SRM Associates
ケーララ州中部全域で認可された医薬品卸売業
SRM Associates は、ケーララ州の認可を受けた医薬品卸売業者です。病院、化学者、薬局に医薬品、医療消耗品、ワクチンを供給しています。
- Type
- Distributor
- Location
- Thrissur, India
- Website
- srmassociates.in
- Categories
- 医薬品製造, 医療およびヘルスケア用品
- Markets
- インド
Verified facts
- lei-active (green), checked 2026-08-07 GLEIF global LEI register (golden copy)
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
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)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)