 |
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 E - Testing Requirements for Relevant Transfusion-Transmitted Infections |
| § 610.39 - Definitions. |
| § 610.40 - Test requirements. |
| § 610.41 - Donor deferral. |
| § 610.42 - Restrictions on use for further manufacture of medical devices. |
| § 610.44 - Use of reference panels by manufacturers of test kits. |
| § 610.45 - Human Immunodeficiency Virus (HIV) requirements. |
| § 610.46 - Human immunodeficiency virus (HIV) “lookback” requirements. |
| § 610.47 - Hepatitis C virus (HCV) “lookback” requirements. |
| § 610.48 - [Reserved] |