Case Study

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


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.

    InCrowd uses the information you provide to us to contact you about our relevant insights, products, and services. You may opt out of communications at any time via the unsubscribe link at the bottom of any email or by sending an email withdrawing your consent to Send Email. For more information, please review our Privacy Policy.
  • This field is for validation purposes and should be left unchanged.