Executive Vice President Technical Operations
- Discuss the current European and US regulatory landscape, and the key differences for manufacturers to be aware of.
- Harmonisation – fact or fiction? Look at the European requirements post 2008, assessing where they fall short of industry requirements and demand
- Plan for the future by predicting further guidelines to emerge and how this will challenge ‘being GMP compliant’
- The Brexit effect! Discuss how the political landscape and changes such as Brexit will alter the GMP requirements
4:30 PM Summative Panel Discussion
Facilitated by the event chair, use this last opportunity to engage with our presenters and audience and ask those
questions you’re still seeking answers to. Based on prior sessions our chairman will also recap the key topic areas of this
year’s forum and take away learnings to make sure you’re driving your therapeutic development forward while we wait
for next year’s summit!