A vaccine recommendation is only as broad as the population it was tested in. This session, timed to the vaccine field's largest meeting, connects the statutory Diversity Action Plan requirement to the site decisions that deliver it: community recruitment, language access, seasonal enrollment speed, and retention through long safety follow-up.
LEARNING OBJECTIVES
- Explain what FDORA requires and where FDA's guidance stands.
- Select sites that can deliver representative vaccine enrollment.
- Plan retention for single-dose studies with long safety follow-up.
Agenda
The Representation Requirement
Community Trust As Enrollment Infrastructure
Poll #1 - Does your next vaccine study carry formal enrollment goals by race and ethnicity?
Language Access And Consent
Enrolling Against The Season
Poll #2 - Where do your vaccine studies lose participants most often?
Retention Through Safety Follow-Up
Q & A - Polling - Handout
Price
Free
Language
English
OPEN TO
Everyone
Dial-in Number
Please register for this Webinar to view the dial-in info.
With 38+ years in the clinical field, Naty leads the organization's strategic growth and multi-site management. Over the past 15 years she has grown Prestige Clinical Research from a single-site operation into an expanding research network across...
With 13+ years of clinical research experience, Samantha oversees multi-site operations, sponsor/CRO engagement, feasibility assessments, business development initiatives, and Investigational Product management. Dedicated to operational...
A Florida-based clinical research network that partners with sponsors, healthcare providers, and local communities to conduct high-quality clinical trials with a dedicated focus on participant safety, regulatory compliance, ethical research...