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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 G
Subpart G—Laboratory Controls
Subpart G. Subpart G—Laboratory Controls
§ 212.60 - What requirements apply to the laboratories where I test components, in-process materials, and finished PET drug products?
§ 212.61 - What must I do to ensure the stability of my PET drug products through expiry?
