61 | How to create a Proactive Postmarketing Surveillance? [EU MDR] 2023-03-21 |
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62 | What you should know about Vigilance Reporting for Medical Devices? 2023-03-14 |
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63 | Medical Device News: March 2023 Regulatory Update 2023-03-08 |
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64 | Prepare your transition from Class I to Class Ir 2023-02-28 |
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65 | SaMD international reach – What to consider? 2023-02-21 |
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66 | Biological Evaluation: Top Big mistakes 2023-02-14 |
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67 | Medical Device News: February 2023 Regulatory Update 2023-02-06 |
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68 | How to do Post-Marketing Surveillance in the US (vs EU)? 2023-01-31 |
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69 | How to evaluate Benefit-Risk Ratio for Medical Devices? 2023-01-24 |
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70 | Breaking News: EU MDR Extension Proposal is out for consultation 2023-01-17 |
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