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Code of Federal Regulations (Last Updated: July 5, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter C - Drugs: General |
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Part 212 - Current Good Manufacturing Practice for Positron Emission Tomography Drugs |
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Subpart G - Laboratory Controls |
§ 212.60 - What requirements apply to the laboratories where I test components, in-process materials, and finished PET drug products? |
§ 212.61 - What must I do to ensure the stability of my PET drug products through expiry? |