TOP AGENDA TOPICS
- Availability of medicines – How to prevent and better mitigate shortages
- Regulatory consequences of Brexit
- Simplifying variations – update on regulatory optimisation
- Implementation phase of the EU/USA Mutual Recognition Agreement (MRA) – How to maximize the benefits
- New ICH quality guidelines under development: Q11 and Q12 – what is new and what impact can be expected?
- Falsified Medicines – what should the regulatory experts know about practical implementation?
- How can patients be provided with up to date and relevant information on their medicines?
- Regulatory challenges for repurposing established medicines
- From junior to senior regulatory affairs – How to shape the best regulatory team
SPECIAL SESSION: Put your questions to the Regulators. An opportunity to address questions to European Regulators!
VISIT US AT BOOTH 2
Did you know that AMPLEXOR Life Sciences is the only partner you need to deliver global market-specific content? From multi-lingual content creation, to content management to publishing, AMPLEXOR Life Sciences provides end-to-end solutions tailored to your needs. Visit our life sciences experts at the booth 3 to learn more!
The Landmark London Hotel
222 Marylebone Road
London NW1 6JQ, UK