General Provisions

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Drugs: General
  6. Current Good Manufacturing Practice for Positron Emission Tomography Drugs
  7. General Provisions

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Section
212.1

What are the meanings of the technical terms used in these regulations?

Section
212.2

What is current good manufacturing practice for PET drugs?

Section
212.5

To what drugs do the regulations in this part apply?