Course Description

CPM: Tracking and Reporting Rules for Medical Device Clinical Trials

Course Description:

The course describes the objectives of establishing tracking and reporting rules during clinical trial setup. It provides guidance on the frequency and types of reporting, as well as methods of detecting deviations in a timely manner so that corrective actions can be put immediately into place.

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Learning Objectives:

Upon successfully completing this course, learners will be able to:

  • Create efficient tracking and reporting rules during setup
  • Detect deviations in time to implement corrective actions

Who Should Enroll:

Clinical project and regulatory managers, senior clinical research associates, and professionals with managerial clinical roles involved in planning and setting up clinical investigations for medical devices are welcome to enroll in this course.

Prerequisite Knowledge/Requirements:

A strong understanding of the flow of clinical investigation projects with specific needs is required for this course.

Subject Matter Expert:
Danielle Giroud

25 min

Related resources:

Case studies:

Basic Account: € 100.00
Premium Account: € 75.00

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