 |
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 F - Biologics |
|
|
Part 610 - General Biological Products Standards |
|
|
Subpart A - Release Requirements |
| § 610.1 - Tests prior to release required for each lot. |
| § 610.2 - Requests for samples and protocols; official release. |