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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 E
Subpart E—Control of Components, Containers, and Closures
Subpart E. 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?
