October 26th - October 28th
This three-day symposium will provide an overview of the current challenges and opportunities in biosimilar development and commercialization, and discuss expectations and requirements from key stakeholders such as manufacturers, physicians, patients and payers.
In this symposium, attendees will:
- Understand the US and European landscape and how APAC developers can bring their biosimilar products to Western markets
- Learn how physician and patient expectations impact the clinical evidence needs critical to trial planning
- Explore the evolution of market demands that influence how we will commercialize biosimilars now and in the future