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FDA Outlines Next Steps For Online Repository And Standard Elements For Device Labeling

Industry representatives, health care providers, patients and caregivers gathered April 29-30 to discuss CDRH labeling activities and the agency’s ideas for the future.

Based on stakeholder input at a workshop on accessible medical device labeling, FDA officials said they will probably develop guidance on the form and content of device labeling and will continue to think about the appropriate scope of an online labeling repository.

The public workshop took place April 29-30 in Silver Spring, Md., and drew industry representatives, health care providers and patients.

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