§ 601.29. Guidance documents.

119 words·~1 min read·/us/cfr/t21/s§ 601.29·

A research copy — for the controlling text, always check the official state or federal source. Not legal advice.

(a)FDA has made available guidance documents under § 10.115 of this chapter to help you comply with certain requirements of this part.

(b)The Center for Biologics Evaluation and Research

(CBER)maintains a list of guidance documents that apply to the center's regulations. The lists are maintained on the Internet and are published annually in the Federal Register. You may request a copy of the CBER list from the Food and Drug Administration, Center for Biologics Evaluation and Research, Office of Communication, Outreach and Development, 10903 New Hampshire Ave., Bldg. 71, Rm. 3103, Silver Spring, MD 20993-0002. [65 FR 56480, Sept. 19, 2000, as amended at 70 FR 14984, Mar. 24, 2005; 80 FR 18092, Apr. 3, 2015]

Connections2 cite this

Cited by 2 sections

Citation graph

cites case law

§ 601.29

Guidance documents.

Fed. Reg.×2

Cites 0Cited by 2 across 1 source