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How to Prepare for Europe’s Medical Device Regulation 2017/745 (EU MDR): Localization Tips and Best Practices

The new European Union Medical Device Regulation (MDR 2017/745) brings significant changes to previous regulations. Device manufacturers who market products in the …

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Streamlining Translation of Adverse Event Reports

Those involved in conducting multi-center clinical trials know that managing Adverse Event (AE) reports received from global trial sites can …

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