---
kind: "section"
citation: "21 C.F.R. § 207.25"
title: "21"
number: "207.25"
heading: "What information is required for registration?"
url: "https://uscodex.org/cfr/21/207.25"
---

# §207.25. What information is required for registration?


Registrants must provide the following information:

- (a) Name of the owner or operator of each establishment; if a partnership, the name of each partner; if a corporation, the name of each corporate officer and director, and the place of incorporation;
- (b) Each establishment's name, physical address, and telephone number(s);
- (c) All name(s) of the establishment, including names under which the establishment conducts business or names by which the establishment is known;
- (d) Registration number of each establishment, if previously assigned by FDA;
- (e) A Unique Facility Identifier in accordance with the system specified under [section 510](/cfr/21/510.md) of the Federal Food, Drug, and Cosmetic Act.
- (f) All types of operations performed at each establishment;
- (g) Name, mailing address, telephone number, and email address of the official contact for the establishment, as provided in [§ 207.69(a)](/cfr/21/207.69.md?p=a); and
- (h) Additionally, with respect to foreign establishments subject to registration, the name, mailing address, telephone number, and email address must be provided for:
  - (1) The United States agent, as provided in [§ 207.69(b)](/cfr/21/207.69.md?p=b);
  - (2) Each importer in the United States of drugs manufactured, repacked, relabeled, or salvaged at the establishment that is known to the establishment; and
  - (3) **Each person who imports or offers for import such drug to the United States.**

## Notes

### Authority

Authority: 21 U.S.C. 321, 331, 351, 352, 355, 360, 360b, 371, 374, 381, 393; 42 U.S.C. 262, 264, 271.

### Source

Source: 81 FR 60212, Aug. 31, 2016, unless otherwise noted.