18 - 20 June, 2018 | Crowne Plaza Zurich, Zurich, Switzerland

Horst Kastrup


Senior Regulatory Advisor
MEDA Pharma


12:20 PM Anti-Counterfeiting Requirements with a Focus on Non-EU Areas

  • Penetrate emerging regions with confidence that you understand their unique regulatory requirements
  • Gain confidence that your products are secure from illegal counterfeiting no matter where they are in the world
  • Develop strategies to help avoid the risk of counterfeiting with clever packaging, labelling & artwork strategies

12:30 PM Airtight EU Regulatory Compliance – Ensuing your Packaging, Labelling and Artwork Strategies are 100% Regulatory Compliant and Inspection Ready

Maintaining 100% regulatory compliance is no easy feat! Knowing the regulations isn’t enough – you need to know how to interpret them, and develop strategies to practically implement them. Moreover, there is increasing pressure on packaging, labelling & artwork professionals to save costs across the entire product life-cycle. Put this all together and meeting regulatory expectations has never been harder.
Attend this workshop to:
  • Overcome the practical challenges of implementing the Falsified Medicines Directive in a cost-effective way
  • Better understand the ISO - standards (IDMP) on pharmaceutical labelling
  • Figure out what best-practice looks like when it comes to tamper evidence packaging features inline with ISO 21296
  • Understand current Good Manufacturing Practice (cGMP) guidelines and principles to avoid any safety issues
  • Decipher the complexities of the global regulatory landscape – know the local differences


Check out the incredible speaker line-up to see who will be joining Horst.

Download The Latest Agenda