Using MedTracS to Combat Falsified Medicines
The FMD directive relating to the control and monitoring of prescription medicinal products and mandatory for all EU Member States entered into force on 09 February 2019.
This new piece of legislation affects all market participants involved in the manufacture, distribution, and sale of prescription medicinal products. In addition to pharmaceutical manufacturers, all pharmaceutical wholesalers, hospitals, and pharmacies have to prepare for the application of this regulation.
The MedTracS software performs control and reporting for medicinal products as part of the serialisation of pharmaceuticals in the entire European Union.
Who is it recommended for
We recommend MedTracS for any participants of the pharmaceutical market, such as
Pharmaceutical wholesalers
MedTracS is a complete and comprehensive FMD solution that meets the logistics needs and requirements of all pharmaceutical wholesalers.
Hospitals
MedTracS is a dedicated FMD solution for any hospital, considering the particularities involved in handling pharmaceuticals and in the logistics processes of the pharmaceutical industry.
Pharmacies
If you represent a pharmacy, MedTracS is a simple and effective solution for you as well, attending to every requirement of the FMD.
Why choose MedTracS?
Professional and state-of-the-art
Developed by leveraging our 30 years of experience in the pharmaceutical and logistics industry.
Continuous technological innovation
MedTracS supports the latest solutions based on market requirements.
Tailored to our customers
MedTracS was developed based on the specific business and legal requirements of pharmaceutical wholesalers, hospitals, and pharmacies.
Complies with regulations
Capable of satisfying all requirements and obligations imposed on our customers by the FMD.
