Do you have a burning regulatory question? Come and get your queries answered with 4 parallel conference tracks:
- Understand the requirements. Successfully register your products. Ensure regulatory compliance in the emerging markets: Russia, CIS countries, Turkey, the Middle East, Africa, LATAM and APAC.
- 18 regulatory agency and industry experts, case studies and interactive sessions to show you the pathway to compliance on IDMP.
- Ensure a robust global submission strategy. Updates from Europe and latest eCTD progress in the GCC, Jordan and China to ensure you meet latest requirements.
- Market access, Business and Commercial Strategies. Regulatory and CMC landscape. Clinical and non-clinical developments: Regulatory agency advice, industry experts and in-depth discussion on biosimilars.
We offer a new central European location, a focused agenda and more opportunities for you to collaborate and connect through a platform for cross-functional discussion.