Implementing a Patient Centered Informed Consent Process (No Contact Hours)

Implementing a Patient Centered Informed Consent Process (No Contact Hours)


Please press the complete button upon completion of the course.

Learning Objectives:

  • Describe the three critical elements of patient-centered care, which are integral to the consent process.
  • List the ways to ensure understanding during the consent process.
  • Develop a personal action plan to improve your organizational policies and procedures around the consent process.

Audience:

This activity is intended for Physicians and Nurses engaged in the care of patients within a clinical research trial.

The activity is also intended for clinical research site personnel.

Knowledge level (basic, intermediate, advanced): Basic

Competency

This course builds competence in the following domains:

  • Clinical Trials Operations (GCPs)
  • Communication and Teamwork
  • Ethical and Participant Safety Considerations

Activities Included:

Implementing a Patient Centered Informed Consent Process (No Contact Hours)

Evaluation