 |
Code of Federal Regulations (Last Updated: November 8, 2024) |
 |
Title 21 - Food and Drugs |
|
|
Chapter I - Food and Drug Administration, Department of Health and Human Services |
|
|
SubChapter C - Drugs: General |
|
|
Part 212 - Current Good Manufacturing Practice for Positron Emission Tomography Drugs |
|
|
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? |