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Informed Consent

Informed Consent

Consultation to guide the development of easy-to-read and understand informed consent documents; patient-specific consent documents may require additional consultation with the CKM health and genetic literacy team

Objective

To equip individuals with the strategies and tools necessary to create effective informed consent documentation for research activities that meet regulatory requirements.  Individuals will learn how to implement best practices for clear communication appropriate to the study population. 

 

Training 

Request a virtual synchronous training:  Request form

 

Primary Contact(s) Credentials

Taneya Y Koonce, MSLS, MPH

Sheila Kusnoor, PhD