Track# |
Workshop Title |
Time |
1 |
Demystifying Real World Evidence Studies |
9:30 am – 5:30 pm |
2
|
Regulatory Pathways for Innovative Clinical Trials |
10:30 am - 1:45 pm |
3
|
From protocol to clinical study report” - Optimizing cross-functional collaboration for authoring protocols and clinical study reports |
9:30 am – 5:30 pm |
4
|
Risk Based Monitoring - Implementation Workshop |
9:30 am – 5:30 pm |
5
|
Concept and Framework of Estimands |
9:30 am – 5:30 pm |
6
|
Safety Aggregate Reports (PSURs / PBRERS) and Risk Management |
9:30 am – 5:30 pm |