21 CFR Part 4 · Regulation of Combination Products

§ 4.100 What is the scope of this subpart?

Subpart B - Postmarketing Safety Reporting for Combination Products Official text on eCFR Amendment history

(a) This subpart identifies postmarketing safety reporting requirements for combination product applicants and constituent part applicants.

(b) This subpart does not apply to investigational combination products, combination products that have not received marketing authorization, or to persons other than combination product applicants and constituent part applicants.

(c) This subpart supplements and does not supersede other provisions of this chapter, including the provisions in parts 314 , 600 , 606 , 803 , and 806 of this chapter , unless a regulation explicitly provides otherwise.

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FDA guidance that cites § 4.100

Amendment history

Federal Register documents that created or amended this section.