Question

The sponsor is responsible for specifying in each protocol the adverse event reporting procedures to be used by those conducting the trial, and to disseminate safety reports to other stakeholders in the research project.

A) Standard Operating Procedures (SOPs)
B) Investigator Brochure
C) Informed Consent Form
D) Protocol

Answer 1

The sponsor in a research project, especially in medicine, is responsible for specifying adverse event reporting procedures and disseminating safety reports to stakeholders.

Step-by-step explanation:

The subject of this question is Medicine. In medical studies, sponsors are responsible for specifying adverse event reporting procedures and disseminating safety reports to other stakeholders in a research project. This ensures the safety of the participants and complies with ethical and legal requirements.