Schedule:
TIME |
Discussion Group Topic Report Outs |
|
8:40 - 9:10 |
Report out on Topic 1: Perceived challenges with FDA/EU/other Regulatory review questions as well as PAIs |
|
9:10 - 9:30 |
Report out on Topic 2: Applicability of Continuous Manufacturing to a Diverse Pharmaceutical Portfolio |
|
9:30 - 9:50 |
Report out on Topic 3: Experience and Technical Capability of Staff to Implement Continuous Manufacturing |
|
9:50 - 10:10 |
Report out on Topic 4: Needed Equipment and Associated Facility Cost |