Critical for any research site is the completion of an SAE form after identification of an adverse event. Although it
Posted: Mon Apr 04, 2022 6:39 am
Critical for any research site is the completion of an SAE form
after identification of an adverse event. Although it
is the responsibility of the PI or clinically identified
investigator, the research staff is often delegated with the
responsibility of completing and preparing the report under the
responsibility of the PI.
after identification of an adverse event. Although it
is the responsibility of the PI or clinically identified
investigator, the research staff is often delegated with the
responsibility of completing and preparing the report under the
responsibility of the PI.