Course Description

The Clinical Investigation Plan

Course Description:

This course provides basic information on the roles and responsibilities of writing clinical investigation plans. It also examines useful tools for monitors to learn about the content of clinical investigation plans.

Learning Objectives:

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

  • Comprehend and interpret clinical investigation plans
  • Achieve a uniform understanding of clinical investigation plan requirements by all parties to ensure subject safety
  • Execute specific clinical investigation plan objectives

Who Should Enroll:

Monitors, clinical project managers, investigators, study coordinators, quality assurance professionals, and regulatory, marketing, and sales professionals wanting to understand the basic requirements of clinical investigation plans are all encouraged to participate in this course. 

Prerequisite Knowledge/Requirements:

The following courses are required:

  • Introduction to Good Clinical Practice (ID 42)
  • Introduction to Medical Device and Clinical Investigation Planning (ID 43)

Subject Matter Expert:
Danielle Giroud

45 min

Related resources:

Case studies:

Basic Account: € 146.00
Premium Account: € 110.00

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