The Clinical Investigation Plan
The Clinical Investigation Plan
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.
ID: 44
45 minutes
2 modules
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
The following courses are required:
- Introduction to Good Clinical Practice (ID 42)
- Introduction to Medical Device and Clinical Investigation Planning (ID 43)
General Requirements for WMDO Courses
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Course Access Duration: Each course is available for 60 days from the date of assignment.
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Quiz Completion: Users are allowed 2 attempts to complete each quiz, with a minimum passing score of 75%.