Webinar: How Compliant Patient Engagement and eConsent Drives Subject-Centricity in 2024

On March 21, 2024, 5thPort hosted a panel discussion on how patient engagement and eConsent impact FDA Audit Preparedness in Clinical Research.
The panelists included: Dr. Sandy Brooks (Virginia Commonwealth University), Dr. Cedron Williams (Advocate Health), and Heather Judge (Rocky Mountain Clinical Research). It was facilitated by Suresh Kumar (SVP, 5thPort). ​
What you will take away with after watching this 5thPort webinar:
1. Gain real-world insights into how to navigate the intricacies and challenges surrounding compliance management - including those related to multiple jurisdictions, languages, and regulatory bodies.
2. Explore how an effective eConsent strategy can mitigate your compliance risk in on-site, decentralized and hybrid trial activities.
3. Identify and track key compliance metrics related to patient engagement and consenting.
4. Learn about preparations you need to make for Diversity, Equity, and Inclusion (DEI) in true patient engagement.
5. A look inside comprehension testing in the consent process - emphasizing factors like time, context and interactions with patients - that meets IRB and FDA regulations and guidelines.
5thPort is a patient engagement and eConsent solution for clinical trials and hospitals. Reach out to us on www.5thPort.com/contact-us/ for a personalized demo.
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