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Code · CFR · Title 21 — Food and Drugs · Part 207 — Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated Under a Biologics License Application, and Animal Drugs, and the National Drug Code · § 207.25

§ 207.25. What information is required for registration?

207 words·~1 min read·/us/cfr/t21/s§ 207.25·

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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 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); 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);
(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.
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§ 207.25
What information is required for registration?
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