Leading patient engagement and eConsent company 5thPort is hosting a webinar on the effects of patient engagement and e-consent on preparedness for FDA audits. The event will take place on Thursday 21 March at 11am ET / 10am CT / 8am PT.
Featuring contributions from Advocate Health, Rocky Mountain Clinical Research, Virginia Commonwealth University and 5thPort, the webinar will dive into the state of clinical trial compliance against the dynamic regulatory landscape of 2024. It will address how simple, standard and transparent digital patient engagement and consenting processes enhance accountability, efficiency, patient education and patient accrual (especially minority accrual) and include real-time statistics around diversity consenting.
Attending the webinar is recommended for the following professionals:
- Clinical trial C-suite executives, including chief compliance officers and chief medical officers
- Regulatory and compliance professionals (regulatory affairs specialists, healthcare privacy officers and compliance officers)
- Heads of clinical research and clinical trial managers
- IRB Chairs, Ethics and Oversight committee members
- Heads of Quality Assurance and Risk Management
For more information about the event and to book a place, please click here. To watch another of our recent webinars, please click here.