HUMAN RESEARCH AND INFORMED CONSENT
Tracking # 20-227531
$99999.00
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Course overview
1. Distinguish human research from other types of research. 2. Identify key events in the history of human research which have led to regulation for protecting research participants. 3. Indicate the purpose, structure, and processes of an Institutional Review Board (IRB). 4. Identify the eight required elements of the informed consent process.
Subject areas
This course counts toward the state boards and subject areas below.
Florida Board of Clinical Laboratory Personnel
Clinical Laboratory Director
1h
General
Clinical Laboratory Supervisor
1h
General
Clinical Laboratory Technician
1h
General
Clinical Laboratory Technologist
1h
General