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DEDICATED TO PROTECTION THROUGH DATA
The CWD Research Initiative is a clinical organization dedicated to the advancement of scientific knowledge and the protection of public health. We advocate for the CWD Equal Protection Act, ensuring that research findings are translated into actionable legislative policies that safeguard communities and preserve the integrity of our research environment.
Our Research Leaders

Dr. Elena Vance
Lead Research Scientist

Dr. Marcus Thorne
Senior Epidemiologist

Sarah Jenkins
Advocacy Director

Dr. Julian Reed
Senior Researcher

Dr. Naomi Chen
Lead Research Scientist

Robert Vance
Advocacy Director
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