# 21 CFR § 20.24: Preparation of new records

> Federal · Regulations · In force

URL: https://www.frixlaw.com/law-library/statutes/ecfr-21-20.24

## Section

- **Citation:** 21 CFR § 20.24
- **Heading:** Preparation of new records
- **Jurisdiction:** Federal
- **Kind:** Regulations
- **Status:** In force
- **Text as of:** September 22, 2026
- **Source:** Publisher's official text
- **Location:** Title 21—Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER A—GENERAL > PART 20—PUBLIC INFORMATION > Subpart B—General Policy

## Text

(a) The Freedom of Information Act and the provisions of this part apply only to existing records that are reasonably described in a request filed with the Food and Drug Administration pursuant to the procedures established in subpart C of this part.
(b) The Commissioner may, in his discretion, prepare new records in order to respond adequately to a request for information when he concludes that it is in the public interest and promotes the objectives of the act and the agency.

## Nearby sections

- [21 CFR § 20.1 § 20.1 Testimony by Food and Drug Administration employees.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.1.md)
- [21 CFR § 20.2 § 20.2 Production of records by Food and Drug Administration employees.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.2.md)
- [21 CFR § 20.3 § 20.3 Certification and authentication of Food and Drug Administration records.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.3.md)
- [21 CFR § 20.20 § 20.20 Policy on disclosure of Food and Drug Administration records.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.20.md)
- [21 CFR § 20.21 § 20.21 Uniform access to records.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.21.md)
- [21 CFR § 20.22 § 20.22 Partial disclosure of records.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.22.md)
- [21 CFR § 20.23 § 20.23 Request for existing records.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.23.md)
- [21 CFR § 20.24 § 20.24 Preparation of new records.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.24.md)
- [21 CFR § 20.25 § 20.25 Retroactive application of regulations.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.25.md)
- [21 CFR § 20.26 § 20.26 Electronic availability and indexes of certain records.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.26.md)
- [21 CFR § 20.27 § 20.27 Submission of records marked as confidential.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.27.md)
- [21 CFR § 20.28 § 20.28 Food and Drug Administration determinations of confidentiality.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.28.md)
- [21 CFR § 20.29 § 20.29 Prohibition on withdrawal of records from Food and Drug Administration files.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.29.md)
- [21 CFR § 20.30 § 20.30 Food and Drug Administration Division of Freedom of Information.](https://www.frixlaw.com/law-library/statutes/ecfr-21-20.30.md)

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Source: Frix Law Library, https://www.frixlaw.com/law-library/statutes/ecfr-21-20.24. Check the current official text before relying on it. Not legal advice.