Alkaloid AD Skopje
المنتجات الصيدلانية ومستحضرات التجميل والكيميائية المصنعة والمصدرة من مقدونيا الشمالية.
Alkaloid هي أكبر شركة أدوية في مقدونيا الشمالية، وتنتج الأدوية العامة ومنتجات الرعاية الصحية التي لا تحتاج إلى وصفة طبية ومستحضرات التجميل التي يتم تصديرها إلى أكثر من 50 دولة. حصلت الشركة على شهادة EU-GMP وتدير خطوط إنتاج متعددة معتمدة تغطي أشكال الجرعات الصلبة والحقن والمنتجات الموضعية.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Skopje, North Macedonia
- Founded
- 1936
- Website
- alkaloid.com.mk
- Categories
- اللوازم الطبية والرعاية الصحية, العناية الشخصية
- Markets
- صربيا, كرواتيا, البوسنة والهرسك, ألبانيا, ألمانيا
Listed in a source registry
Macedonian exporters directory
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
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
- debarment-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- product-authorised-for-sale (green), checked 2026-08-21 Ministry of Health of Armenia, State Register of Medicinal Products (pharm.am)
- certificate-page-on-site (amber), checked 2026-09-18 Company's own certification page
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- Good Manufacturing Practice
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)