DIGITAL SUMMIT: ACCELERATING FDA DIVERSITY ACTION PLANS
In light of the updated draft guidance on DAPs, we are bringing pharmaceutical companies, biotechs, and medical device companies from around the world the critical intel to ensure scientifically representative clinical studies are delivered.
WHY JOIN US?
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EXPERT INSIGHT
Hear leading experts’ thoughts on the updated guidance and how they tackle barriers to recruitment, retention, and inclusive research.
OPTIMIZE GOALS
Optimize your goal setting procedures with rigorous epidemiologically backed data science approaches.
ENGAGE UNDERSERVED POPULATIONS
Deploy effective all-encompassing measures to engage underserved populations in clinical studies including community engagement, accessibility, burden-reduction, education, awareness and more.
LEVERAGE VENDORS
Learn how to utilize vendors and ecosystem partners to improve representation.
CLINICAL TRIAL SPONSOR INFORMATION
The new FDA guidance on Diversity Action Plans requires sponsors to set recruitment goals backed by rationale and epidemiological evidence to increase patient diversity in clinical trials relating to sex, gender, age, ethnicity and race as well as other relevant underrepresented populations. Hear insights from sponsors on assembling effective DEI strategies in practice and efforts to build inclusivity into clinical research.
Relevant Functions Include:
DEI & Clinical Trial Diversity
Real World Evidence
Epidemiology
Trial Optimization
Study Leads
Patient Engagement, Recruitment & Retention
Clinical Operations
Clinical Operations
Clinical Development
Medical Affairs
Medical Science
Medical Writing
Patient Marketing
Marketing & Commercial
About Kisaco Research
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