Pr-041872 Re-Consenting Research Subjects
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Type
Presentation
Credit
No
Description
Covers how to identify when re-consent is needed (e.g., new risks), how to obtain IRB-approved consent ... show more
Covers how to identify when re-consent is needed (e.g., new risks), how to obtain IRB-approved consent forms, methods for contacting subjects, and the requirement for documenting the re-consent process and securing the subject’s updated signature. show less
Objectives
- To ensure that research subjects continue to give voluntary, informed consent after new or significant information is available [Procedure MG.O-004.04]
Fees
Free
Faculty
Candice Vance
Organization
MedStar Health Research Institute