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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 A - General Provisions |
| § 212.1 - What are the meanings of the technical terms used in these regulations? |
| § 212.2 - What is current good manufacturing practice for PET drugs? |
| § 212.5 - To what drugs do the regulations in this part apply? |