A new training program from the Association of Clinical Research Professionals (ACRP) allows site teams and monitors to role-play the informed consent process.

In ACRP’s interactive Informed Consent Simulation course, learners participate in a variety of scenarios as patients, study coordinators, investigators and monitors to gain an understanding of the process from all viewpoints. The course is designed to develop the core competencies needed to properly conduct and document the informed consent process.

Individual and organizational licenses are available, with organizational licenses including a reporting system that helps identify areas for improvement.

To learn more about the course, click here: https://bit.ly/2PesrKw.