21 C.F.R. · Food and Drugs
21 C.F.R. § 4.104

How and where must you submit postmarketing safety reports for your combination product or constituent part?

Title 21 C.F.R. ● ACTIVE Primary Source
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21 C.F.R. § 4.104 — How and where must you submit postmarketing safety reports for your combination product or constituent part?

§ 4.104 How and where must you submit postmarketing safety reports for your combination product or constituent part? (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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21 C.F.R. § 4.104
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The regulatory text of 21 C.F.R. § 4.104 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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