21 C.F.R. · Food and Drugs
21 C.F.R. § 4.3

What current good manufacturing practice requirements apply to my combination product?

Title 21 C.F.R. ● ACTIVE Primary Source
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21 C.F.R. § 4.3 — What current good manufacturing practice requirements apply to my combination product?

§ 4.3 What current good manufacturing practice requirements apply to my combination product? If you manufacture a combination product, the requirements listed in this section apply as follows: (a) The current good manufacturing practice requirements in parts 210 and 211 of this chapter apply to a combination product that includes a drug constituent part; (b) The current good manufacturing practice requirements in part 820 of this chapter apply to a combination product that includes a device constituent part; (c) The current good manufacturing practice requirements among the requirements (including standards) for biological products in parts 600 through 680 of this chapter apply to a combination product that includes a biological product constituent part to which those requirements would apply if that constituent part were not part of a combination product; and (d) The current good tissue practice requirements including donor eligibility requirements for HCT/Ps in part 1271 of this chapter apply to a combination product that includes an HCT/P.

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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BS-CFR21-SEC-DA692E
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21 C.F.R. § 4.3
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The regulatory text of 21 C.F.R. § 4.3 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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