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HumanSubjectsProtection,EthicalResearch and IRB

Overview:

This two day seminar will provide the foundation for the application, concepts and theories of clinical research. Within the two days, attendees will learn about the historical evolution of research, current regulations and guidelines including the Common Rule, FDA regulations and HIPAA. We will discuss site and study staff responsibilities in the conduct and reporting of research, types of studies and the regulatory requirements that apply to different study designs. We will discuss a variety of research including genetic, drug, device, and studies that use off-site or community partners. Current examples will be used and the audience will be invited to share their experiences and information.



Event Coordinator
Toll free: 800-385-1607
Fax: 302 288 6884
Email: [email protected]
Event Link: http://bit.ly/RDgVcb
Website: http://www.mentorhealth.com


Human Subjects Protection Ethical Research IRB

On July 24 2014 at United States 5 Views





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