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Consumers head to court on OTC cold pills

Now that the FDA’s outside experts have determined the meds’ active ingredient is ineffective, regulators must decide whether to pull many of the most popular nonprescription cold meds off store shelves. ....

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The Voluntary Improvement Program FDA Seeks Public Comment On Draft Guidance

The FDA seeks comments on its proposed guidance describing its policy regarding FDA's participation in the Voluntary Improvement Program. The. ....

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The Voluntary Improvement Program FDA Seeks Public Comment On Draft Guidance

The FDA seeks comments on its proposed guidance describing its policy regarding FDA's participation in the Voluntary Improvement Program. The. ....

Mark Durivage , Device Discovery Appraisal Program , Requirements Development , Drug Administration , Improvement Program , Radiological Health , Product Quality Pilot Program Cfq , Quality Systems Compliance , Device Innovation Consortium , Fostering Medical Device Improvement , Voluntary Improvement , Voluntary Improvement Program , Medical Device Innovation Consortium , Capability Maturity Model Integration , Medical Device Discovery Appraisal Program , Federal Food , Organizational Excellence , Quality Voluntary Medical Device Manufacturing , Product Quality Pilot Program , Cfq Pilot Program , Information Systems Audit , Control Association , Bruce Tuckman , Dockets Management Staff ,

FDA tightens authorized use of J&J's Covid-19 vaccine- POLITICO

The vaccine is still available under emergency use authorization, and the CDC has already made a preferential recommendation for the mRNA vaccines over J&J’s. ....

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