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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 |
|---|---|---|---|---|---|
| The Lifecycle of Medical Devices from Idea to Market | Recommended | 42 mins | € 136.00 | € 102.00 |
| 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 | |
| The European Union Regulatory System for Medical Devices | Recommended | 175 mins | € 517.00 | € 388.00 | |
| Demarcation of Medical Devices to Other Products | Recommended | 60 mins | € 195.00 | € 146.00 | |
| Integrating Risk Management into Your Quality Management System | Recommended | 35 mins | € 118.00 | € 88.00 | |
| Introduction to Process Validation | Recommended | 75 mins | € 243.00 | € 183.00 | |
| Project Management of Medical Device Development | Recommended | 85 mins | € 374.00 | € 281.00 | |
| ISO 13485:2016 - Medical Devices Quality Management Systems Requirements for Regulatory Purposes | Recommended | 183 mins | € 403.00 | € 303.00 | |
| Overview of US FDA Quality System Regulation | Recommended | 75 mins | € 330.00 | € 248.00 |
| Course Title Click on a title to view course description | Status | Duration | Basic | Premium | Purchase |
|---|---|---|---|---|---|
| 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 | |
| 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 | |
| Standalone Software Under the Medical Devices Directives | Recommended | 40 mins | € 160.00 | € 120.00 | |
| Validating Software used in Company Processes | Recommended | 65 mins | € 260.00 | € 195.00 |
| 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 | |
| Introduction to Good Clinical Practice | Recommended | 45 mins | € 99.00 | € 75.00 | |
| Format and Structure of a Medical Device Clinical Investigation Plan/Protocol | Recommended | 42 mins | € 145.00 | € 109.00 | |
| Clinical Protocol Writing Process and Ensuring Compliance | Recommended | 35 mins | € 121.00 | € 91.00 | |
| ISO 14155:2020 – A Summary Review | Recommended | 80 mins | € 260.00 | € 195.00 | |
| 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 |
|---|---|---|---|---|---|
| Pathways to CE Marking under the In Vitro Diagnostics Directive | Recommended | 50 mins | € 148.00 | € 111.00 |