With over 16,000 medical device recalls in 2024 affecting more than 70 million devices worldwide, the challenges around executing recalls are bigger than ever.
Traditionally, device recalls rely on spreadsheets, manual outreach, and slow response cycles. But in today’s world—where patients, regulators, and the media demand speed and accountability—those methods just don’t cut it anymore.
In our latest blog post, “Medical Device Recalls: the impact of disruptive, digital technology on Device Recalls” we explore:
Why conventional recall processes strain commercial, quality, and regulatory teams
Five key areas in recall lifecycles where digital tools can make the biggest difference
How digital tools can mitigate for a poorly executed product Recall
If you’re responsible for device safety, regulatory compliance, or quality assurance, this read offers a fresh lens on how digitization can turn a reactive process into a proactive strength.
We’d also love to help you think through your recall strategy—how digital tools could fit, where to start, and what’s realistic for your operations. If you’d like to explore, let’s get a call on the calendar.
Best regards,
Andrew Vincent
Offering Lead, Recalls & Field Services
IQVIA MedTech
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