It’s been one year since the European Union adopted the Falsified Medicines Directive as a means of combatting counterfeiting in the pharmaceutical industry. What has changed after EU FMD for the Parallel Traders?
In this webinar, SoftGroup’s Track & Trace experts will focus the attention on the issues that still need to be addressed, including the requirements and responsibilities for Pharma Parallel Importers, how the main process is happening as well as some key points for Pharmaceutical Parallel Traders and best practices.
The webinar will take place on 30 April, at 4 p.m. CET.
What to expect?
- Requirements and responsibilities for Pharma Parallel Importers
- How the main process is happening?
- Falsified Medicines Directive in Europe: Key points for Pharmaceutical Parallel Traders
- Best practices
The webinar will include a question and answer session, during which participants will have an opportunity to interact with the webinar speaker to question or clarify any of the issues surrounding the EU FMD.