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Current Good Manufacturing Practice for Positron Emission Tomography Drugs

  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

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Subpart
A

General Provisions

Subpart
B

Personnel and Resources

Subpart
C

Quality Assurance

Subpart
D

Facilities and Equipment

Subpart
E

Control of Components, Containers, and Closures

Subpart
F

Production and Process Controls

Subpart
G

Laboratory Controls

Subpart
H

Finished Drug Product Controls and Acceptance

Subpart
I

Packaging and Labeling

Subpart
J

Distribution

Subpart
K

Complaint Handling

Subpart
L

Records

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