CFR > Title 21 - Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER C—DRUGS: GENERAL (parts 200 to 299) > PART 212—CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS > SUBPART H—Finished Drug Product Controls and Acceptance (§212.70 to §212.71)

SUBPART H—Finished Drug Product Controls and Acceptance (§212.70 to §212.71)