| Introduction to Emergency Research |
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The RAMPART and ProTECT studies will be conducted using special rules for studies in which the subjects are too sick or incapacitated to either agree to or decline to participate at the time they are being treated in the ambulance or in the Emergency Room.To learn more about these rules, referred to as "exception from informed consent for emergency research" click here.
Part of the EFIC (exception from informed consent) process is releasing study information to the community in which the study will be deployed. This allows the community to provide feedback, ask questions, share comments and opt out of inclusion in the study. In this webpage, you will learn about our efforts on community consultation and public disclosure.
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