Issues with Consent Documents 2015

Topics

• Plain Writing
• Information on Health Literacy
• Increasing readability
• Consent as a process
• Exculpatory language
• 6 - 8th grade examples
• What IRB reviewers like and dislike
• Tips for using consent templates

Who should Attend

• Clinical Research Scientists (PKs, Biostatisticians,)
• Principal Investigators / Sub-investigators
• Clinical Research Associates (CRAs) and Coordinators (CRCs)
• Safety Nurses
• QA / QC Auditors and Staff
• Recruiting Staff
• Human Research Protection Professionals
• Clinical Research Data Managers