Voices From Within: Humanizing Clinical Research Data: Episode 1 – Patient Data Collection 101

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 article brief here.

Watch Webinar Episodes 2 & 3
Voices From Within: Humanizing Clinical Research Data:
Episode 2 – Patient Data Collection 101 Flash Webinar
Voices from Within: Humanizing Clinical Research Data: Episode 2- Conversations on DCTs: Data Privacy
Voices from Within: Humanizing Clinical Research Data:
Episode 3 – Conversations on Clinical Trials
Voices from Within: Humanizing Clinical Research Data: Episode 3- Conversations on Clinical Trials