HIPAA Compliant 2014 - HIPAA Compliant Research: From Recruitment to Study Closure

Overview: There are unique rules for HIPAA compliance for research that are important for all researchers and study staff to be aware of before undertaking any projects that handle PHI. This presentation will cover HIPAA compliance in research from the very beginning of the recruitment process, during consent, and even after study closure. The speaker will also address research involving deceases patients and limited data sets. Sign up to make sure you understand how to be compliant with the HIPAA requirements for research.
Why should you attend: Is your research HIPAA compliant? Do you understand how HIPAA applies to research? Do you understand the difference between HIPAA compliance in clinical care and research?
Areas Covered in the Session:
An overview of HIPAA Compliance for research
HIPAA pitfalls during recruitment
Consent for Research- handling HIPAA
Study Closure and Post-Study data collection and HIPAA compliance
Research involving deceased patients
Research involving limited data sets
Who Will Benefit:
Principal Investigators
Coordinators
Research Staff
Research Nurses
Research Compliance Individuals
IRB Members
IRB Staff
Research Project Managers
Claire Carbary has worked as an attorney for commercial IRBs for seven years. Ms. Carbary joined Quorum Review IRB in September of 2009 as a Regulatory Attorney in Quorum Review’s Regulatory Department. Prior to working at Quorum, Ms. Carbary worked as a Regulatory Analyst and Legal Intern at Western IRB. Ms. Carbary received her Certified IRB Professional certification in 2010. She currently serves as a member of the Northwest Association for Biomedical Research (NWABR) and Public Responsibility in Medicine and Research (PRIM&R).
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