MedTech Intelligence

Top MedTech Summer Stories

By MedTech Intelligence Staff
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MedTech Intelligence

Following protocols and maintaining compliance have been common themes.

With Labor Day behind us, the traditional American summer has come and gone. Despite the light reading that many summer lovers seek, the audience of MedTech Intelligence was interested in learning more about EU MDR and product design, among other critical topics. Read on to view the most popular stories of the season.

5. New MDR: One Year into the Transition Period

New MDR: One Year into the Transition Period

4. Simplifying Medical Device Labeling in a Complex Environment

Simplifying Medical Device Labeling in a Complex Environment

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

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

Learn more about this important regulation by attending the EU MDR: Implementation Strategies Workshop November 27–28, 2018. Attend in-person or virtually!

2. Stop Validating Computer Systems to Death!

Stop Validating Computer Systems to Death!

1. What Healthcare Professionals Don’t Want in a Medical Device

What Healthcare Professionals Don’t Want in a Medical Device

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