CPM: Project Guidelines for Medical Device Clinical Trials
Course Description:
This course provides an outline of project guideline objectives, content, and maintenance for clinical investigations with medical devices.
Learning Objectives:
Upon successfully completing this course, learners will be able to:
- Ensure cooperative teamwork and homogenous data for final reports within a designated deadline
- Write efficient project guidelines to improve teamwork and enhance the managerial skills of clinical investigation project managers
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 all welcome to participate in this course.
Prerequisite Knowledge/Requirements:
The following courses are required:
- CPM: Objectives and Setup of a Medical Device Clinical Trial (ID 97)
- CPM: The Clinical Trial Master Plan for Medical Devices (ID 98)
- CPM: Medical Device Clinical Trials – Budget and Timeline Planning (ID 99)
- CPM: Medical Device Clinical Trial Team Resources (ID 100)
- CPM: Tracking and Reporting Rules for Medical Device Clinical Trials (ID 101)