Course Description

CPM: The Clinical Trial master plan for Medical Devices

Course Description:

This course navigates the strategic objectives of clinical trial master plans and how they are written and maintained. It outlines the importance and subtlety of a well-written clinical trial master plan and how it is used within the contexts of marketing and medical device company business objectives.

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Learning Objectives:

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

  • Define and demonstrate the basic principles and objectives of effective project management for clinical investigations
  • Identify and comprehend the different milestones within a clinical investigation

Who Should Enroll:

Product, clinical project, and regulatory managers, and professionals with managerial clinical roles involved in planning strategic clinical evaluation programs for medical devices are all encouraged to enroll in this course.

Prerequisite Knowledge/Requirements:

The following material is required:

  • Understanding of the basics of good clinical practices
  • Familiarity with clinical quality systems
  • Basic knowledge of the regulatory requirements involved in conducting clinical investigations

Subject Matter Expert:
Danielle Giroud

50 min

Related resources:

Case studies:

Basic Account: € 200.00
Premium Account: € 150.00

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