The age of paper has passed and eConsent is becoming an increasingly popular method to obtain informed consent in clinical investigations. The benefits of using eConsent in clinical investigations become clear to many companies as they replace outdated paper-processes.
This webinar will answer the most common questions on eConsent in medical device clinical investigations.
By watching the webinar you will learn about:
- Best practices for eConsent in clinical investigations
- The three ways of obtaining eConsent
- GDPR compliance pitfalls when implementing eConsent
- Answers to the most frequently asked questions about eConsent
Keywords: eConsent, Clinical Investigations, GDPR Compliance
Jón I Bergsteinsson
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