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Code of Federal Regulations (Last Updated: November 8, 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 E - Control of Components, Containers, and Closures |
| § 212.40 - How must I control the components I use to produce PET drugs and the containers and closures I package them in? |