§314.445. Guidance documents.
21 C.F.R. § 314.445
FDA has made available guidance documents under § 10.115 of this chapter to help you to comply with certain requirements of this part.
The Center for Drug Evaluation and Research (CDER) maintains a list of guidance documents that apply to CDER's regulations. The list is maintained on the Internet and is published annually in the Federal Register. A request for a copy of the CDER list should be directed to the Office of Training and Communications, Division of Drug Information, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993-0002.
Notes, amendments, and revision history
Amendments
[65 FR 56480, Sept. 19, 2000, as amended at 74 FR 13113, Mar. 26, 2009]
Source
Source: 50 FR 7493, Feb. 22, 1985, unless otherwise noted. Redesignated at 57 FR 17983, Apr. 28, 1992.
Authority
Authority: 21 U.S.C. 321, 331, 351, 352, 353, 355, 355a, 355f, 356, 356a, 356b, 356c, 356e, 360cc, 360ddd, 360ddd-1, 371, 374, 379e, 379k-1.
Source
Source: 50 FR 7493, Feb. 22, 1985, unless otherwise noted.
Amendments
[65 FR 56480, Sept. 19, 2000, as amended at 74 FR 13113, Mar. 26, 2009]