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    FDA Revises Draft Guidance on Certification Process for Medical Gases

    The revisions on the 2012 draft guidance on the certification process for medical gases includes new discussions on the labeling for final use containers and what documentation is necessary for marketers of a medical gas that are not the original manufacturer or marketer. The revisions are in response to comments made on the initial guidance on certifying medical gases, though FDA says it doesn’t believe the changes will have too much of an impact on industry. Labe...