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Course Title Click on a title to view course description | ID | Duration | Basic | Premium | Purchase |
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Role of RA Specialist in the Design Process | 154 | 40 mins | |||
Pre-Market Approval for Medical Device in China | N139 | 53 mins | |||
The European Medical Device New Regulation 2017/745 | N180 | 330 mins | € 925.00 | € 694.00 | |
Current and upcoming IVD market access requirements in Europe | |||||
The Draft European IVD Regulation | N181 | 50 mins |
Course Title Click on a title to view course description | ID | Duration | Basic | Premium | Purchase |
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Understanding Clinical Evaluation for Notified Body and Regulatory Professionals | |||||
Clinical Evaluation Report: Review for Regulatory Professionals | 107 | 70 mins | € 308.00 | € 231.00 |
Course Title Click on a title to view course description | ID | Duration | Basic | Premium | Purchase |
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ISO 13485:2016 - Medical Devices Quality Management Systems Requirements for Regulatory Purposes | 196 | 183 mins | € 403.00 | € 303.00 | |
Overview of US FDA Quality System Regulation | 118 | 75 mins |
Course Title Click on a title to view course description | ID | Duration | Basic | Premium | Purchase |
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Preparing Successfully for a US FDA Medical Device Inspection | 215 | 109 mins |
Course Title Click on a title to view course description | ID | Duration | Basic | Premium | Purchase |
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Powerful Presentation Skills | 70 | 140 mins |
Course Title Click on a title to view course description | ID | Duration | Basic | Premium | Purchase |
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Effective Time Management | N148 | 176 mins |
Course Title Click on a title to view course description | ID | Duration | Basic | Premium | Purchase |
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CMDA Clinical Evaluation - Mock Exam | N131 | 90 mins | € 90.00 | € 90.00 |