21 C.F.R. · Food and Drugs
21 C.F.R. § 500.86

Marker residue and target tissue.

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 500.86 — Marker residue and target tissue.

§ 500.86 Marker residue and target tissue. (a) For each edible tissue, the sponsor shall measure the depletion of the residue of carcinogenic concern until its concentration is at or below S m . (b) In one or more edible tissues, the sponsor shall also measure the depletion of one or more potential marker residues until the concentration of the residue of carcinogenic concern is at or below S m . (c) From these data, FDA will select a target tissue and a marker residue and designate the concentration of marker residue (R m ) that the regulatory method must be capable of measuring in the target tissue. FDA will select R m such that the absence of the marker residue in the target tissue above R m can be taken as confirmation that the residue of carcinogenic concern does not exceed S m in each of the edible tissues and, therefore, that the residue of carcinogenic concern in the diet of people does not exceed S o . (d) When a compound is to be used in milk- or egg-producing animals, milk or eggs must be the target tissue in addition to the tissue selected to monitor for residues in the edible carcass. (Approved by the Office of Management and Budget under control number 0910-0228)

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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21 C.F.R. § 500.86
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The regulatory text of 21 C.F.R. § 500.86 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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