Webinar pharma serialization 2015: Current status in the EU, Brazil, Saudi Arabia and Russia.
Drug safety and falsified medicines are the top issues in the pharmaceutical industry, and face marketing authorization holders with significant challenges. The EU announced for mid-2015 the delegated act for the directive 2011/62/EU. With Brazil and Saudi Arabia two other countries will start in 2015 with the serialization of medicinal products. But also Russia is engaged with plans for the introduction of a relevant legislation.
In two separate webinars, which were organized in cooperation with the BITKOM Akademie and the arvato Systems GmbH, Mr. Tobias Beer from ACS PharmaProtect GmbH gave a lecture about the current status of the European legislation, and the associated requirements for marketing authorization holders.
In the focus of the webinar were furthermore the following topics:
- Brazil: The hardest serialization law of the world starts already in this year!
- Saudi Arabia: On April 1, 2015 Saudi Arabia starts. What has to be considered?
- Russia: How far is Russia advanced with the serialization?
The available participation places of the webinar were booked in a very short time. The expectations of the auditorium of this series of events were entirely fulfilled. The very positive feedback encouraged us to plan additional dates for future webinars.
These dates will given due notice by the usual distribution list of the ACS PharmaProtect GmbH.