Best of 2024: #6 Article – Closing the global product information gap

Regulatory affairs can fuel clinical and quality teams with key product information, help speed time to market, and be a catalyst for innovation. But the truth is most medtechs aren’t seeing these benefits, slowed down by inefficient administrative tasks.

Figure 1: Most medtech regulatory professionals don’t have direct access or a single source to access global documents for in-country submissions.
Figure 1: Most medtech regulatory professionals don’t have direct access or a single source to access global documents for in-country submissions.
COURTESY OF VEEVA MEDTECH

Posted by Elizabeth Engler Modic, Editorial Director - Manufacturing Group

Published December 26, 2024
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The countdown is now at the #6 most read article from 2024 and it's all about regulatory! You need to know how to manufacture precision medtech devices but the regulatory landscape is just as important.

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