Register now: March 16, 2016 – 3rd securPharm Infoday on the Falsified Medicines Directive

The legislative process for the delegated act, which makes the technical and organisational provisions for the realisation of the Falsified Medicines Directive for the protection of the patients is nearly completed. The roadmap is clear: In three years from now the demanded safety measures have to be implemented in whole Europe.  After this date only prescription medication with the new safety features shall be placed on the market.

For pharmaceutical undertakings the furnishing of its products with an individual serial number and the respective data upload for the verification are a challenge, not only from a technical point of view. The content of the delegated regulation creates in many aspects transparency, but adds as well many new questions of detail.  On March 16, 2016 at the 3rd Infoday Falsified Medicines Directive in Frankfurt am Main, Germany you will have the chance to discuss your questions with experts.

Intended audience of this event are employees of pharmaceutical companies and interested wholesalers and pharmacists.  Main topic is the labelling of the medicines with the new safety features. Other topics like the application of the coding rules at packaging and printing are explained by experts of ACS PharmaProtect – operator of the database system of the pharmaceutical industry at securPharm- in detail, like the steps of the internal measures for a successful data upload. Practitioners of the pharmaceutical supply report of their experiences of the serialisation of medicines and the changeover of complete production lines. At the Infoday representatives of the ministry of health and the EU-Commission will take part in person and are available for questions.

The conference language will be German.

Registration details and other information can be found under the website www.securPharm.de/events. The event is liable to costs. The registration fee for pharmaceutical companies, pharmacists and wholesalers are 490 € plus VAT per person. Representatives from public authorities and institutes which fulfill public tasks regarding the safety of patients are free of charge. Other participant groups are charged with the price of 2000 € plus VAT per person.

The program you can view here.

Venue:

Kap Europa
Osloer Straße 5
60327 Frankfurt am Main
Germany

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