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IMPACT 1077HS (AIDS Document ID 10779) HEART Standard Version of the PROMISE Study (Promoting Maternal and Infant Survival Everywhere) A Multi center, US Domestic and International Trial of the International
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The IMPAACT 1077HS DAIDS document is a form used to report adverse events during clinical trials.
Principal investigators and sponsors of clinical trials are required to file the IMPAACT 1077HS DAIDS document.
The IMPAACT 1077HS DAIDS document should be filled out with details of any adverse events experienced by participants in the clinical trial.
The purpose of the IMPAACT 1077HS DAIDS document is to ensure the safety of participants in clinical trials by reporting and tracking adverse events.
The IMPAACT 1077HS DAIDS document must report details of the adverse event, the participant involved, the severity of the event, and any actions taken.
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