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Impact and Interventions Related to FDASIA: Increasing Diversity in Clinical Trials
Program Code:
419
Date:
Thursday, June 27, 2013
Time:
10:45 AM to 12:15 PM
EST
CHAIR
:
Brenda Jamerson,
Campbell University College of Pharmacy and Health Sciences, United States
Brenda Jamerson, PharmD is Associate Professor Campbell University College of Pharmacy, Director Clinical Research Center and VAMC GRECC Research Pharmacist. She was previously Director Depression/Dependence at GlaxoSmithKline with responsibilities for program development in the neurosciences area.
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SPEAKER
(S):
Brenda Jamerson, PharmD (SCHSUP), Associate Professor, Clinical Research, Campbell University College of Pharmacy and Health Sciences, United States
Almenia K. Garvey,
MSc (SPKNON), Senior Clinical Feasibility Leader,
PAREXEL International, United States
Almenia received a Bachelor’s from UNC-Chapel Hill, and a Masters from the University of Ulster, Northern Ireland. She has 16 years of experience in site selection strategy, investigator identification and investigator relationship management. Ms. Garvey specializes in minority site recruitment.
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Rebecca Lynn Budd, (SPKNON), Managing Director, Navita Clinical Strategy Group, United States
Description
This symposium will provide an overview of the FDA Safety and Innovation Act (FDASIA) addressing the challenges and strategies related to increasing minority enrollment in clinical trials and the strategies that may facilitate comprehension of Informed Consent.