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Electronic Informed Consent in clinical trials has
been highlighted as a topic of interest at recent eClinical Forum meetings. The
technology demonstration provided a good insight into the functional
capabilities, business opportunities and challenges of eICF systems.
Our thanks go to Scott Askin, Novartis, Switzerland
and to Eric Delente, DrugDev, USA who facilitated a very interesting webinar.
Slides used during the event can be downloaded by eCF
members.
The session explored in detail:
- How eICF can improve how we engage, manage and
monitor patients involved in clinical trials
- The change management challenges
- How such Digital Technologies can make a significant
difference
- The functionality offered by one eICF system offered
by Enforme Interactive/Drug Dev’s SecureConsent Application
- Measured improvements in comprehension and process
control
- The steady growth in use and experience
- Best practices, business value and Regulatory
acceptance