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

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