TÜV Rheinland Blog - Insights from Asia and Africa
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Ensuring Medical Device Effectiveness and Safety

By Bhavya H M, Sr. Executive, Business development, TÜV Rheinland India
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TÜV Rheinland: Notified Body for the New Medical Device Regulation

TÜV Rheinland LGA Products GmbH is now a notified body for the EU Medical Device Regulation (MDR) 2017/745 / Introduction of Eudamed central database / Increased requirements for notified bodies.
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A Wireless Medical Device May Have a Great Design, But Is It Safe?

Device manufacturers are usually familiar with proper design methods for devices, but often get lost navigating through the standards and regulations necessary for developing wireless medical ...
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Common Requirements for X-Ray Diagnostic Equipment

  Since the discovery of radiation and radioactivity more than 100 years ago, radiation protection standards and the philosophy governing those standards have evolved. Proper evaluation of these ...
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