Cybersecurity, COVID-19 and EU MDR Hot Topics of the 2020 MedTech Summer

10

Risk Management and Other Cybersecurity Considerations for Connected Medical Devices

9

What Patients Expect Out of Their Wearable Medical Devices

8

Preparing for MDR: Don’t Forget about Class I Reusable Devices

7

Trends in Medical Device Recalls

6

Patent and Regulatory Challenges in AI’s Use in Life Sciences

5

EU MDR Post-Market Surveillance: Active, Integrated, Risk-Based, and Planned

4

EU MDR Supplier Quality Requirements: Convergence of Best Practice and Regulation

3

Medical Device Cybersecurity in the Age of IoMT

2

Corrections, Corrective Actions, and Preventive Actions: Effectively Handling Nonconformances in Compliance with the EU MDR

1

Full Economic Impact of COVID-19 on Life Sciences Industry Still Uncertain

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