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8 Cards in this Set
- Front
- Back
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What are the federal agencies involved in the residueprogram |
FDA, USDA, EPA |
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•Identifythe key components of an agricultural chemical and drug approval for foodanimals |
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•Describekey components of the USDA-FSIS residue monitoring program |
-all animals slaughtered at federally inspected plants have the potential of being sampled (random sampling) which produces a statistically valid national drug residue pic -3 or more individual tissue samples are taken from a single animal -sample at a rate that will detect a 1% incidence w/an assurance of 99% --requires 800 randomly collected samples evenly spaced over the yr -fsis reports illegal drug residue to fda - |
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•Describethe use of in-plant and on-farm tests that can be utilized for antimicrobialdetection |
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•Identifythe most common causes of residues and how to avoid them |
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How does FDA regulate residue |
-Animal drug manufacturers show that each new animal drug is safe and effective -manufacturers submit a reliable assay method for detecting drug residues in slaughtered animals -analytical methods are reviewed by FDA and FSIS before the drug is approved -Sets tolerances for acceptable lvls of residues of the drug in animal tissue |
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how does EPA regulate residue |
-Responsible for approving pesticides use on animals -similar t FDA, establishes a safe limit or tolerance -Establishes a withdrawal pd if needed -approves assay method for detecting pesticide residues in meat, milk, and eggs if needed |
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how does usda fsis |
-monitors tissue samples from slaughtered animals for presence of chemical compounds -FA w/residues above the tolerance lvls are considered adulterated -takes enforcement action as needed |
