§ 4.3. What current good manufacturing practice requirements apply to my combination product?
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/us/cfr/t21/s§ 4.3A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
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 other than a medical gas;
(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;
(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; and
(e)The current good manufacturing practice requirements in part 213 of this chapter apply to a combination product that includes a drug constituent part that is a medical gas. [78 FR 4321, Jan. 22, 2013, as amended at 89 FR 51766, June 18, 2024]
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§ 4.3
What current good manufacturing practice requirements apply to my combination product?
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