3 Part Flash Webinar Series
There are a variety of ways in which patient data can be collected in clinical research. As such, it’s critical to keep patients informed on these methods as they progress through trials. Jane Myles, Curebase’s VP of Clinical Trial Innovation and Director of Data Management, Kim Andreasen, discuss how patient data is collected in clinical trials.
View the webinar below. View article brief here.
Watch Webinar Episodes 2 & 3
Voices from Within: Humanizing Clinical Research Data:
Episode 2 – Conversations on DCTs: Data Privacy
Watch Here
Voices from Within: Humanizing Clinical Research Data:
Episode 3 – Conversations on Clinical Trials
Watch Here
Panelists:
Jane Myles
VP, Clinical Trial Innovation at Curebase
Kim Andreasen
Director, Data Management at Curebase
