Servicepoint and Systech: Our view for the Falsified Medicines Directive


Servicepoint and Systech have followed closely the progress of European pharmaceutical manufacturers regarding their process of meeting the set European Falsified Medicine Directive deadline. The companies have published an update on the current situation and progress.

With only one year to go the EU FMD deadline of Feb 9, 2019, is approaching fast. This means that there is only a year of implementation time left. While big pharma has largely implemented serialization, medium and small manufacturers, as well as CMOs and virtual pharmas, are lagging in beginning their implementation.

Servicepoint is one of the few companies with the skills and resources to integrate serialization to an existing production line, thus retrofit.

Servicepoint has done more than a dozen serialization integration projects ranging geographically from France to Russia.  Our experience with Systech’s UniSeries serialization solutions platform gives us the flexibility and confidence to help any European manufacturer serialize, and meet the February 2019 deadline.

The partnership between Servicepoint and Systech gives a combined 60+ years of experience for customers to rely on as  Systech has experience of over 30 years in packaging and serialization software and Servicepoint’s production line experience provides another 30  years of experience.

You can read the complete article here.

Iiro Jantunen
CTO, Chief Technology Officer
Servicepoint Kuopio Oy