Policy establishing joint committees

The safety and health committee will participate in periodic inspections to review the effectiveness of the safety program and make recommendations for improvement of unsafe and unhealthy conditions. This committee will be responsible for monitoring the effectiveness of this program. The committee will review safety inspection and accident investigation reports and, where appropriate, submit suggestions for further action. 

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The U.S. Food and Drug Administration policy is based on the conclusions of the Joint FAO/ WHO Expert Committee on Food Additives (JECFA). In its Thirty-Second Report (1988), it concluded, on the basis of its safety assessment of residues of estradiol-17/3, progesterone, and testosterone, and in view of the difficulty of determining the levels of residues attributable to the use of these hormones as growth promoters in cattle, that it was unnecessary to establish an acceptable residue level. As to trenbolone acetate (TBA), a synthetic steroid with anabolic properties, JECFA concluded that its safety assessment could be based on establishing the no-hormonal-effect level. It therefore recommended a maximum residue level of 2 /zg/kg for /3-tren-bolone in meat and of 10 /xg/kg for a-trenbolone in liver on the basis of a daily intake by a 70-kg person of 500 g of meat. /3-Trenbolone is the major metabolite in muscle. For zeranol, an acceptable residue level of 10 /xg/kg for bovine liver and 2 /zg/kg for bovine muscle was established. 

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