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Medtech industry report reveals state of content and claims across commercial
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The 2025 Medtech Regulatory Affairs Benchmark reveals that many companies lack confidence in the completeness or accuracy of data and still rely heavily on manual processes to maintain compliance. These challenges are driving medtechs to embrace unified regulatory information management (RIM) systems, data, and AI tools.
Key findings include:
55% Indicate it would take significant time and effort
to find where a product is registered globally
50% Are only somewhat or not at all confident their data
includes all relevant registration information
67% Have partially or entirely manual processes for
monitoring key metrics
56% Plan to adopt a RIM system to improve efficiency
and compliance
Download the full report for more insights on the state of regulatory affairs and how medtech companies are working to prioritize automation, strengthen data governance, and adopt advanced technologies.
Copyright © 2025 Veeva MedTech | Newsletter
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