Hemofarm a.d.
Хемофарм а.д. производит дженерики для готовых к экспорту каналов B2B.
Хемофарм а.д. производит дженерики, стерильную продукцию и фармацевтические препараты во Вршаце. Основанная в 1960 году, компания снабжает аптеки, больницы, дистрибьюторов медицинских товаров и экспортные рынки в RS, BA, MK, DE и связанных с ними экспортных рынках.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Vrsac, Serbia
- Founded
- 1960
- Website
- hemofarm.com
- Categories
- Медицинские товары и расходники
- Markets
- Сербия, Босния и Герцеговина, Северная Македония, Германия
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
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- product-authorised-for-sale (green), checked 2026-08-21 Ministry of Health of Armenia, State Register of Medicinal Products (pharm.am)
- sanctions-clear (green), checked 2026-08-12 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-12 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- domain-registered (green), checked 2026-08-12 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)