| Regulatory Rapporteur October 2020 (full issue) | MEMBERS |
| Regulatory approval of medical device software and digital health devices | MEMBERS |
| An overview of advanced therapy regulation – part I: the EU | MEMBERS |
| Regulatory affairs strategic planning: how to do it well | MEMBERS |
| Devices without a medical purpose: how do they fit into the MDR? | MEMBERS |
| Interview: Lessons for a full lifecycle in pharma | MEMBERS |
| Current use of artifificial intelligence in the MedTech industries | MEMBERS |