29 January 09:00 - 29 January 16:30
A seminar on serialization in the pharmaceutical industry.
The European Parliament adopted in 2011 a comprehensive EU directive on falsified medicines, Directive 2011/62/EU, to prevent counterfeit medicines from entering the legal supply chain. This directive requires a comprehensive system in form of serialization, an "electronic pedigree”, to track and monitor the route of prescription drugs. Different instances of the industry have requested a forum for discussion and exchange of knowledge due to the EU legislation and the readjustment this will mean for all parts of the industry.
The purpose of this day is to work as a forum for discussion and information-sharing within the pharmaceutical industry. Based on extent of the new EU directive, it is important that the entire chain gather and have the opportunity to discuss this challenge and start working from an overall perspective of traceability.
We expect around 100 participants from pharmaceutical companies, equipment manufacturers, distribution- and packaging companies.
Moderator: Torkel Gren, Recipharm
Date: January 29, 2015
Place: Skogshem & Wijk, Lidingö
Time: 9.00-16.20
Chartered bus runs from 8.00 City terminal (see information boards for the gate number). The return trip takes place after program completion (16.30) by alighting at the City Terminal.
Registrering