With more international markets moving towards electronic submissions as well as the specific requirements from EU agencies, it is essential that you are up to speed with latest requirements and expectations.
Informa Life Sciences 11th Annual Global eCTD Management conference brings together both European and international regulatory agency and industry speakers to ensure that you take away the latest information on global progress towards eCTD, EU telematics, European regulatory agency feedback, implications of the new EU Clinical Trial Regulation (Regulation No 536/2014) on submissions and much more.
2015 Conference Highlights:
- Feedback from 4 key Notified Bodies
- Competent Authority feedback
- Focus on post market surveillance data
- Benchmark your regulatory strategy with your peers...
- Examining success strategies for proactive post market surveillance
- 3 additional interactive workshops