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
€39
€419

Purchase

Essential

3
Premium
–
–
–
–
1
Unlimited
€149
€1590

Purchase

Pro

Unlimited
Proactive
–
–
–
Multiple
Unlimited
€319
€3390

Purchase

Enterprise

Unlimited
Managed
Multiple
Unlimited
Ask Quotation
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

Purchase

Essential

FMD Transactios & Compliance
Mobile & Web App up to 3 devices
Bulk Verification
Premium Support
–
–
–
–
Unlimited Scans
1 User
€110 Monthly
€1210 Yearly

Purchase

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

Purchase

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

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)