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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 |
|---|---|---|---|---|---|
| ISO 14971: 2007 Review | Recommended | 35 mins | € 118.00 | € 88.00 | |
| Preparing Risk Management File & Which Techniques Apply | Recommended | 24 mins | € 80.00 | € 61.00 | |
| Integrating Risk Management into Your Quality Management System | Recommended | 35 mins | € 118.00 | € 88.00 | |
| European Safety Reporting Requirements during Clinical Investigations | Recommended | 25 mins | € 74.00 | € 55.00 | |
| US Safety Reporting Requirements during Pre-Market Clinical Trials | Recommended | 20 mins | € 65.00 | € 48.00 |
| Course Title Click on a title to view course description | Status | Duration | Basic | Premium | Purchase |
|---|---|---|---|---|---|
| Format and Structure of a Medical Device Clinical Investigation Plan/Protocol | Recommended | 42 mins | € 145.00 | € 109.00 | |
| Designing a Strategic Medical Device Clinical Investigation Plan/Protocol | Recommended | 90 mins | € 499.00 | € 375.00 | |
| Clinical Protocol Writing Process and Ensuring Compliance | Recommended | 35 mins | € 121.00 | € 91.00 |
| Course Title Click on a title to view course description | Status | Duration | Basic | Premium | Purchase |
|---|---|---|---|---|---|
| Clinical Evaluation for Market Approval | Recommended | 80 mins | € 352.00 | € 264.00 | |
| Clinical Evaluation Report: Review for Regulatory Professionals | Recommended | 70 mins | € 308.00 | € 231.00 | |
| Data from Prospective Clinical Investigation for CE-Mark: Review for Regulatory Professionals | Recommended | 95 mins | € 418.00 | € 314.00 | |
| Biological Evaluation of Medical Devices: A Risk-Based Approach | Recommended | 63 mins | € 205.00 | € 158.00 | |
| Complaint Handling and Reporting Process for Medical Devices | Recommended | 65 mins | € 211.00 | € 158.00 | |
| How to Navigate Through the ISO 13485 Certification Process | Recommended | 44 mins | € 194.00 | € 145.00 |
| Course Title Click on a title to view course description | Status | Duration | Basic | Premium | Purchase |
|---|---|---|---|---|---|
| Conducting Medical Device Clinical Investigations in Germany | Recommended | 85 mins | € 374.00 | € 281.00 | |
| Conducting Medical Device Clinical Investigations in Switzerland | Recommended | 35 mins | € 107.00 | € 80.00 |