Walsh M
European Commission, Directorate-General for Health and Consumer Protection, Brussels, Belgium.
Food Addit Contam. 2000 Jul;17(7):637-9. doi: 10.1080/026520300412564.
The question of the variability of pesticide residues and acute risk assessment has arisen in the context of the work of the European Commission's Scientific Committee for Plants (SCP). A brief outline is presented of European Community legislation on pesticide residues and the authorization of plant protection products. It is stated that although chronic risk assessment is systematically carried out in connection with the fixing of Community MRLs, the same has not applied for acute risk assessment. The reasons for this situation have been the absence of an agreed methodology, acute reference dose (RfD) and adequate dietary and residue data. It is stated that in the opinion of the Scientific Committee for Plants an acute risk assessment should be considered on a routine basis and that steps should be taken to ensure the availability of the necessary data. Possible implications for risk communication and the authorization of plant protection products in the EC are also discussed.
农药残留的变异性问题以及急性风险评估是在欧盟委员会植物科学委员会(SCP)的工作背景下出现的。本文简要概述了欧盟关于农药残留和植物保护产品授权的立法。文中指出,虽然在确定欧盟最大残留限量(MRLs)时系统地进行了慢性风险评估,但急性风险评估却并非如此。出现这种情况的原因是缺乏商定的方法、急性参考剂量(RfD)以及足够的膳食和残留数据。植物科学委员会认为,应常规性地考虑急性风险评估,并应采取措施确保必要数据的可得性。文中还讨论了这对欧盟风险沟通和植物保护产品授权可能产生的影响。