Your Trusted Partner in Diagnostics
Why Choose Antfarma
We combine regulatory expertise, manufacturing excellence, and pan-European logistics to deliver diagnostic solutions that healthcare professionals and distributors can rely on.
Our Numbers Speak
Seven years of consistent growth in the regulated diagnostics space, serving partners across the European Union.
CE/IVD
Full Regulatory Compliance
All products comply with IVDR 2017/746 and carry CE marking for in vitro diagnostics
ISO 13485
Certified Manufacturing
All products manufactured in ISO 13485 and ISO 9001 certified facilities with full traceability
50+
Diagnostic Products
Comprehensive portfolio covering respiratory, infectious disease, cardiac, GI, and drug testing
33
European Countries
Distribution network spanning 33 countries via GIRP-affiliated wholesale partners
Built for Scale
B2B Clients Across Europe
From national pharmacy chains to independent distributors, healthcare institutions, and retail networks.
Years in Regulated Diagnostics
Deep expertise navigating IVDR compliance, CE marking processes, and market-specific registration requirements.
Warehouses in Vilnius
24-hour dispatch for in-stock items with reliable cold-chain and ambient logistics across the EU.
Dispatch Time
Same-day or next-day dispatch for all in-stock items, with priority handling for institutional orders.
What Sets Us Apart
Direct Manufacturer Access
No middlemen. Direct relationships with CE-certified manufacturers mean better pricing, faster supply, and full documentation access.
Complete Regulatory Dossier
Declaration of Conformity, Technical Documentation, Performance Evaluation Reports, and market-specific registration support included.
Private Label Capability
Launch your own branded diagnostic line. Full OEM service from concept to CE-marked product with your branding.
Dedicated Account Management
Every partner gets a dedicated contact for orders, inquiries, regulatory questions, and marketing support.
Marketing & POS Support
Professional product photography, digital assets, planogram support, and co-marketing opportunities for retail partners.
Certifications & Compliance
Every product in our portfolio meets the highest European regulatory standards for in vitro diagnostics.
CE/IVD Marking
All products carry the CE mark for in vitro diagnostic medical devices under Regulation (EU) 2017/746 (IVDR).
ISO 13485 & ISO 9001
Manufacturing partners hold both ISO 13485 (medical devices QMS) and ISO 9001 (quality management) certifications.
ISO 45001
Occupational health and safety management system certification ensuring safe working conditions throughout the supply chain.
Ready to Partner With Us?
Whether you're a pharmacy chain, distributor, healthcare institution, or looking for private label solutions — we'd love to discuss how we can support your business.