To evaluate the safety and efficacy of a new treatment

To compare two or more existing treatments

To gather information about a disease or condition

To test the effectiveness of a new medical device

Phase I, Phase II, Phase III, Phase IV

Phase A, Phase B, Phase C, Phase D

Phase 1, Phase 2, Phase 3, Phase 4

Phase X, Phase Y, Phase Z, Phase W

To evaluate the safety of a new treatment

To determine the effectiveness of a new treatment

To compare a new treatment to an existing treatment

To gather information about a disease or condition

To evaluate the safety of a new treatment

To determine the effectiveness of a new treatment

To compare a new treatment to an existing treatment

To gather information about a disease or condition

To evaluate the safety of a new treatment

To determine the effectiveness of a new treatment

To compare a new treatment to an existing treatment

To gather information about a disease or condition

To evaluate the safety of a new treatment

To determine the effectiveness of a new treatment

To compare a new treatment to an existing treatment

To gather information about a disease or condition

Informed consent, confidentiality, and risk-benefit assessment

Data collection, data analysis, and data interpretation

Study design, study conduct, and study monitoring

Publication of results, dissemination of results, and implementation of results

To review and approve clinical trial protocols

To monitor the conduct of clinical trials

To ensure the safety and well-being of clinical trial participants

All of the above

To review safety data from clinical trials

To make recommendations to the study sponsor regarding the continuation or termination of a clinical trial

To ensure the safety and well-being of clinical trial participants

All of the above

To design and conduct the clinical trial

To fund the clinical trial

To oversee the conduct of the clinical trial

All of the above

To conduct the clinical trial

To recruit participants for the clinical trial

To collect data from clinical trial participants

All of the above

To assist the clinical investigator with the conduct of the clinical trial

To recruit participants for the clinical trial

To collect data from clinical trial participants

All of the above

To design the clinical trial

To analyze the data from the clinical trial

To interpret the results of the clinical trial

All of the above

To review the ethical aspects of the clinical trial protocol

To provide guidance to the IRB on the ethical issues related to the clinical trial

To educate clinical trial participants about the ethical issues related to the clinical trial

All of the above