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title 21
Food and Drugs
chapter I-i3
CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
part 212
PART 212—CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
subpart A
Subpart A—General Provisions
Subpart A. 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?