Case Study
Cardiovascular Device Company Exceeds Patient Enrollment Goals Six Months Ahead of Schedule
Sep 04, 2023
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Learn how a medical device company scaled its post-market trial for cardiovascular grafts and patches to meet new EU MDR requirements during the global pandemic.

With a flexible approach, IQVIA MedTech used its cardiovascular post-market clinical experience to exceed patient enrollment goals six months ahead of schedule.

Discover how IQVIA MedTech:

  • Activated 31 sites across seven countries 
  • Helped the sponsor maintain EU MDR compliance on five legacy medical devices
  • Leveraged its therapeutic area expertise to enroll and retain over 1,600 patients for a post-market cardiovascular trial that required long-term follow-up

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