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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 I
Subpart I—Packaging and Labeling
Subpart I. Subpart I—Packaging and Labeling
§ 212.80 - What are the requirements associated with labeling and packaging PET drug products?
