Hemofarm a.d.
هيموفارم أ.د. تقوم بتصنيع أدوية عامة لقنوات B2B الجاهزة للتصدير.
هيموفارم أ.د. تقوم بتصنيع الأدوية العامة والمنتجات المعقمة والتركيبات الصيدلانية في فرساك. تأسست الشركة في عام 1960، وتقوم بتزويد الصيدليات والمستشفيات وموزعي الرعاية الصحية وأسواق التصدير عبر RS وBA وMK وDE وأسواق التصدير ذات الصلة.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Vrsac, Serbia
- Founded
- 1960
- Website
- hemofarm.com
- Categories
- اللوازم الطبية والرعاية الصحية
- Markets
- صربيا, البوسنة والهرسك, مقدونيا الشمالية, ألمانيا
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)