| Section No. | Description |
|---|---|
| Section 4.1 | How does FDA define key terms and phrases in this subpart? |
| Section 4.2 | What current good manufacturing practice requirements apply to my combination product? |
| Section 4.3 | How can I comply with these current good manufacturing practice requirements for a co-packaged or single-entity combination |
| Section 4.4 | Headquarters |