Verifarma Wholesalers is a flexible and complete solution designed specifically for pharmaceutical wholesalers to be in compliance with the EU FMD requirements.
In order to supply medicinal products in Europe after 9th February 2019 and complete the end-to-end verification, distributors may need to be able to accomplish the verification and decommission of medicinal products at higher risk of falsification in the repositories system.
As expert’s technology providers for the pharmaceutical industry, with Verifarma Wholesalers we help pharmaceutical wholesalers across Europe to cost-effectively ensure compliance with the FMD to minimise the risk of falsified medicinal products.
When should I verify the authenticity of the unique identifier of a medicine?
Hospital
Those received from suppliers by the central pharmacy of the hospital.
Pharmacy
Those received by suppliers
Functionalities – FMD Transactions
Scan 2D data matrix barcode.
Verification of both the authenticity of the unique identifier and the integrity of the anti-tampering device.
Decommissioning of the unique identifier of medicinal products which are:
- Supplied to the public. Supplied status.
- Distributed outside the Union. Export status.
- Intended for destruction. Destroyed status.
- Requested as samples by competent authorities. Sample status.
- Returned products which cannot be returned to saleable stock. Locked status.
- Intends to distribute to the persons or institutions referred to in Article 23*, where required by national legislation in accordance with the same Article.
- Mark as stolen. Stolen status.
Revert the status of a decommissioned unique identifier to an active status if the conditions described in the article 13 of the Commision Delegated Regulation (EU) 2016/161 are fulfilled.
Possibility of manual entry the unique identifier code.
Connection to the National Medicine Verification System of the respective countries.
Register all events and FMD transactions.
Key features
Mobile and web access
Integrations with client’s ERP
Rapidly adaptation at regulatory updates
Cost-effective solution for large, small and medium companies.
Certified quality standards.
How to buy it
Verifarma for Hospital and Pharmacy | Plans
Feature
- FMD Transactions & Compliance
- Mobile & Web App devices
- Bulk Verification
- Support
- Multi User and Multi Site
- ERP Integration & Aggregation
- Enterprise Security and Audits
- Dedicate Project Management
- Users
- Scans
- Monthly
- Yearly
Single
- 1
- Ticketing
- –
- –
- –
- –
- 1
- Unlimited
- €29
- €319
Essential
- 3
- Premium
- –
- –
- –
- –
- 1
- Unlimited
- €110
- €1210
Pro
- Unlimited
- Proactive
- –
- –
- –
- Multiple
- Unlimited
- €260
- €2860
Enterprise
- Unlimited
- Managed
- Multiple
- Unlimited
- Ask Quotation
- Ask Quotation
How to buy it
Verifarma for Wholesalers | Plans
Single
- FMD Transactios & Compliance
- Mobile & Web App up to 1 devices
- Bulk Verification
- Ticketing Support
- –
- –
- –
- –
- Unlimited Scans
- 1 User
- €29 Monthly
- €319 Yearly
Essential
- FMD Transactios & Compliance
- Mobile & Web App up to 3 devices
- Bulk Verification
- Premium Support
- –
- –
- –
- –
- Unlimited Scans
- 1 User
- €110 Monthly
- €1210 Yearly
Pro
- FMD Transactios & Compliance
- Mobile & Web App unlimited devices
- Bulk Verification
- Proactive Support
- Multi User and Multi Site
- –
- –
- –
- Unlimited Scans
- Multiple Users
- €260 Monthly
- €2860 Yearly
Enterprise
- FMD Transactios & Compliance
- Mobile & Web App unlimited devices
- Bulk Verification
- Managed Support
- Multi User and Multi Site
- ERP Integration & Aggregation
- Enterprise Security and Audits
- Dedicate Project Management
- Unlimited Scans
- Multiple Users
- Monthly Ask Quotation
- Yearly Ask Quotation
Countries where we operate
Contact us for more information and advice
Why Verifarma?
Focus on Regulations
Regulatory know how, we update our services on the basis of the regulations in force in each market.
Quality and Standards
ISO Standards.
Members of GS1 since 2013
24-hours Customer Service
Personalized service, 365 days a year, in Spanish, English and Portuguese.
International solution
With 13 years’ experience and more than 2000 active implementations in 20 countries.
Experience in connections with regulatory entities
ANMAT (Argentina)
SENASA (Argentina)
SEDRONAR (Argentina)
ANVISA (Brazil)
EMVO (Europe)
CRPT (Russia)
SEVEM (Spain)
KOWAL (Poland)
MVO (France)
PAvlina Stisova (Czech Republic)