Presented by Tamara Howard. 

What: Brief presentations on topics such as IRB Updates, Clinical Trial Recruitment, Clinical Trial Billing, Best Budget Practices, Informed Consenting, HIPAA Regulations, and more. 

Why: The goal of this program is to fill any gaps in information related to the implementation of clinical trials that have been identified by investigators and their research teams. 

Who: Seminar topics will be of interest and relevance to clinical research personnel including investigators, regulatory personnel, study coordinators and financial administrators. *CME credits provided for each session.