Case Study

How Real-Time Global Data Supports Post-Market Surveillance Requirements for Medical Device Companies

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A medical device client needed to develop an efficient approach that satisfied the EU MDR and FDA requirements for actively collecting direct feedback from users for their approved in-market devices.

Read this case study to learn how InCrowd’s real-time, global quantitative services helped one medical device company gauge cardiac nurse reactions and receive feedback about their new in-market product.

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