Hemofarm a.d.
Hemofarm advertentie produceert generieke medicijnen voor exportgerichte B2B-kanalen.
Hemofarm advertentie produceert generieke medicijnen, steriele producten en farmaceutische formuleringen in Vrsac. Het bedrijf werd opgericht in 1960 en levert aan apotheken, ziekenhuizen, gezondheidszorgdistributeurs en exportmarkten in RS, BA, MK, DE en aanverwante exportmarkten.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Vrsac, Serbia
- Founded
- 1960
- Website
- hemofarm.com
- Categories
- Medische en gezondheidszorgbenodigdheden
- Markets
- Servië, Bosnië en Herzegovina, Noord-Macedonië, Duitsland
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)