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Ethics, Regulations and Study Implementations for Research Involving Human Subjects
(Health)

Presentations will include Ethics of research,investigational drugs,Device development, informed consent,monitoring trials, GCP,HIPAA, IRB, Researh Integrity & compliance, minority population, recruitment & retention, study selection, contract& budget negotiation, conflict of interest,Federal Regulations, cultural competency in clinical trials,etc. Registration is free and will be limited to 35 participants. Sponsored by the REKS.component of the Georgetown-Howard Universities Center for Clinical and Translational Science (GHUCCTS)

Location: Georgetown University, Warwick-Evans
Price: Free
Sponsor: Georgetown-Howard UniversitiesCenter for Clinical &Translational Science, Regulatory Component
Contact: Jane Otado
E-Mail j_otado@howard.edu
202-865-4881
Mar 2013
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