 |
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 A - General |
|
|
Part 4 - Regulation of Combination Products |
|
|
Subpart A - Current Good Manufacturing Practice Requirements for Combination Products |
| § 4.1 - What is the scope of this subpart? |
| § 4.2 - How does FDA define key terms and phrases in this subpart? |
| § 4.3 - What current good manufacturing practice requirements apply to my combination product? |
| § 4.4 - How can I comply with these current good manufacturing practice requirements for a co-packaged or single-entity combination product? |