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The following curriculum of courses have been determined by WMDO experts to help you to reach your career objectives according to the position you have selected and are divided into sections which will allow you to follow the proposed training in an efficient and structured manner.
For this reason, we strongly recommend that you complete each section before moving along to the next.
| Course Title Click on a title to view course description | Status | Duration | Basic | Premium | Purchase |
|---|---|---|---|---|---|
| History of Good Clinical Practice (GCP) | Recommended | 15 mins | FREE | FREE | |
| The Informed Consent Process | Recommended | 45 mins | € 146.00 | € 110.00 | |
| Introduction to Good Clinical Practice | Recommended | 45 mins | € 99.00 | € 75.00 | |
| Adverse Event Processes | Recommended | 77 mins | € 218.00 | € 163.00 | |
| ISO 14155:2020 – A Summary Review | Recommended | 80 mins | € 260.00 | € 195.00 | |
| US Safety Reporting Requirements during Pre-Market Clinical Trials | Recommended | 20 mins | € 65.00 | € 48.00 | |
| Format and Structure of a Medical Device Clinical Investigation Plan/Protocol | Recommended | 42 mins | € 145.00 | € 109.00 | |
| European Safety Reporting Requirements during Clinical Investigations | Recommended | 25 mins | € 74.00 | € 55.00 | |
| Clinical Evaluation of Medical Devices: an Introduction | Recommended | 43 mins | € 127.00 | € 95.00 | |
| Clinical Protocol Writing Process and Ensuring Compliance | Recommended | 35 mins | € 121.00 | € 91.00 | |
| Ethics Committee(EC) / Institutional Review Board Requirements | Recommended | 40 mins | € 130.00 | € 98.00 |