An E2E or EE2 consultation will review the evidence required by various stakeholders, such as regulators, payers, patients, healthcare providers, and physicians. This information will be incorporated into the design of a prospective study.
The consultation may include:
- working with the investigator to design a study that includes both efficacy and effectiveness endpoints,
- providing advice on suitable populations to include in the effectiveness phase of the trial,
- creating a statistical analysis plan, and
- identifying the role of the Data Safety Monitoring Board in moving from the efficacy to the effectiveness phase.