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Code of Federal Regulations Title 21. Food and Drugs § 21.4.104 How and where must you submit postmarketing safety reports for your combination product or constituent part?

Current as of January 02, 2025 | Updated by Findlaw Staff

(a) If you are a constituent part applicant, you must submit postmarketing safety reports in accordance with the regulations identified in § 4.102(b) that are applicable to your product based on its application type.

(b) If you are a combination product applicant, you must submit postmarketing safety reports required under § 4.102 in the manner specified in the regulation applicable to the type of report, with the following exceptions:

(1) You must submit the postmarketing safety reports identified in § 4.102(c)(1)(i) and (ii) in accordance with § 314.80(g) of this chapter if your combination product received marketing authorization under an NDA or ANDA or in accordance with § 600.80(h) of this chapter if your combination product received marketing authorization under a BLA.

(2) You must submit the postmarketing safety reports identified in § 4.102(c)(2)(ii) and (c)(3)(ii) in accordance with § 803.12(a) of this chapter if your combination product received marketing authorization under a device application.

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Cite this article: FindLaw.com - Code of Federal Regulations Title 21. Food and Drugs § 21.4.104 How and where must you submit postmarketing safety reports for your combination product or constituent part? - last updated January 02, 2025 | https://codes.findlaw.com/cfr/title-21-food-and-drugs/cfr-sect-21-4-104/

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