CFR section
21 CFR 58.130(c): Conduct of a nonclinical laboratory study
PART 58-GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES · Subpart G-Protocol for and Conduct of a Nonclinical Laboratory Study
Key facts
| Citation | 21 CFR 58.130(c) |
|---|---|
| Section | Conduct of a nonclinical laboratory study |
| Part | PART 58-GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES |
| Subpart | Subpart G-Protocol for and Conduct of a Nonclinical Laboratory Study |
| Subchapter | 21 CFR A General |
| Product types cited | General |
| Regulation text (excerpt) | (c) Specimens shall be identified by test system, study, nature, and date of collection. This information shall be located on the specimen container or shall accompany the specimen in a manner that precludes error in the recording and storage of data. |
At a glance
- 10–99 Inspections citing this section
- 1–9 Warning letters citing this section
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About CFR sections cited by the FDA
Title 21 of the Code of Federal Regulations contains the FDA's regulations, including current good manufacturing practice and quality system requirements that inspections cite.