The Pharma Regulations and Technical MasterClass will support you in collecting, sorting and proper understanding of the requirements of the EU Falsified Medicines Directive, the Worldwide Serialisation Requirements and Artwork ;
This includes the relevant information related to the defined two EU-safety features, which are a unique identifier and tamper evident closures to be applied to the packaging of medicinal products within the EU starting 9th February 2019. Also, this course will deal with the existing and emerging global serialization and track and trace requirements for medicines and their packaging in markets such as China, Korea, US, and others.
By the end of the MasterClass, the participants will understand:
i) The Requirements for EU-Falsified Medicines Directive 2019
ii) The Serialisatons Effects and consequences
iii) EU Falsified Medicines Directive
iv) Artwork Management
v) Digital Content Management
For the training description, detailed trainer profile and training program, please request the Training Agenda.
|Building:||Falkensteiner Hotel Am Schottenfeld|
|Address:||Schottenfeldgasse 74 1070 Vienna Austria|
|Type:||Course & Training|