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国际食品法典农药残留标准制订程序
热度 1 wcwcsong 2011-4-11 23:14
国际食品法典农药残留标准制订程序 所有食品法典标准都主要在其各分委员会中审议、制定,然后经 CAC 大会审议后通过。法典标准都是以科学为基础,并在获得所有成员国的一致同意的基础上制定出来的,有一般程序和加速程序两种制定程序。 一般程序 第 1 步 确定标准制定计划。 该计划由 CAC 根据 CAC 执行委员会的审查结果决定,并确定由 CCPR 承担标准制定工作;也可由 CCPR 提出,但需经 CAC 批准。 第 2 步 提出标准建议草案。 秘书处安排起草标准建议草案,在制订农药 MRL 时,由 JMPR 提出 MRLs 建议草案及开展残留风险评估工作的其他相关信息。 第 3 步 征求意见。 将标准建议草案送交 CAC 成员国和相关国际组织,征求其对所有方面的意见,包括标准建议草案可能对经济利益的影响。 第 4 步 CCPR 会议审议。 秘书处将收到的意见转交 CCPR 大会进行审查。 第 5 步 提交 CAC 大会审议。 标准建议草案通过秘书处转交执行委员会审查并提交 CAC 大会审议通过,成为一项标准草案。 第 6 步 再次征求意见。 标准草案由秘书处送交 CAC 成员国和相关国际组织,征求对所有问题的意见,包括标准草案可能对其经济利益的影响。 第 7 步 CCPR 会议再次审议。 秘书处将收到的意见转交 CCPR 大会再次审查。 第 8 步 提交 CAC 大会审议。 标准草案连同从成员国和相关国际组织收到的任何书面意见,通过秘书处转交执行委员会严格审查并提交 CAC 大会,审议通过后成为法典标准。 Procedures for the Elaboration of Codex Standards on Pesticide Residues All Codex standards are considered and developed in the Committees and adopted by the Commission after deliberation at its Plenary Session, where they are endorsed by consensus among all member countries. They are established on scientific basis through the Uniform Procedure and the Uniform Accelerated Procedure. The Uniform Procedure: Step 1 Propose to elaborate a standard. CAC decides on the proposal to set a standard taking into account the outcome of the critical review conducted by the Executive Committee, and also decides CCPR should undertake the work. The proposal can also be put forward by CCPR, subject to the subsequent approval by CAC. Step 2 Make available a proposed draft standard. The Secretariat arranges for the preparation of a proposed draft standard. In the case of MRL for pesticides, JMPR makes available the recommendations of MRL and any other relevant information regarding residue risk assessment work it conducted. Step 3 Call for Comments. The proposed draft standard is sent to CAC members and interested international organizations for comment on all aspects including possible implications of the proposed draft standard for their economic interests. Step 4 Consideration by CCPR. The comments received are sent by the Secretariat to CCPR for consideration at its annual Session. Step 5 Review by the Commission. The proposed draft standard is submitted through the Secretariat to the Executive Committee for critical review and to the Commission with a view to its adoption as a draft standard. Step 6 Call for second round of comments. The draft standard is sent by the CAC Secretariat to all its members and interested international organizations for comments on all aspects, including possible implications of the draft standard for their economic interests. Step 7 Reconsideration by CCPR. The comments received are sent by the Secretariat to CCPR for reconsideration at its annual Session. Step 8 Adoption by the Commission. The draft standard is submitted through the Secretariat to the Executive Committee for critical review and to the Commission, together with any written proposals received from members and interested international organizations, with a view to its adoption as a Codex standard. 加速程序 第 1 步 CAC 应根据执行委员会严格审查的结果和大会表决的三分之二多数票,确定哪些标准可以采用加速程序。也可根据 CCPR 会议表决的三分之二多数票来确定,但需经 CAC 批准。 第 2 步 提出标准建议草案。 秘书处安排起草标准建议草案,在制订农药 MRL 时,由 JMPR 提出 MRLs 建议草案及开展残留风险评估工作的其他相关信息。 第 3 步 征求意见。 将标准建议草案送交 CAC 成员国和相关国际组织,征求其对所有方面的意见,包括标准建议草案可能对经济利益的影响。 第 4 步 CCPR 会议审议。 秘书处将收到的意见转交 CCPR 大会进行审查。 第 5 步 提交 CAC 大会审议。 标准建议草案通过秘书处转交执行委员会审查并提交 CAC 大会审议通过,成为一项法典标准。 农药残留限量法典标准的制定过程是由 JMPR 评估并提出建议值, CCPR 讨论通过提交当年的 CAC 大会讨论通过后,发布为 CAC 标准,如不能通过,则循环审议。 The Accelerated Procedure Step 1 The Commission, on the basis of a two-thirds majority of votes cast, taking into account the outcome of the critical review conducted by the Executive Committee, shall identify those standards which shall be the subject of an accelerated elaboration process. The identification may also be made by CCPR on the basis of a two-thirds majority of votes cast at its Session, subject to the confirmation by the Commission. Step 2 Make available a proposed draft standard. The Secretariat arranges for the preparation of a proposed draft standard. In the case of MRL for pesticides, JMPR makes available the recommendations of MRL and any other relevant information regarding residue risk assessment work it conducted. Step 3 Call for Comments. The Proposed draft standard is sent to CAC members and interested international organizations for comment on all aspects including possible implications of the proposed draft standard for their economic interests. Step 4 Consideration by CCPR. The comments received are sent by the Secretariat to CCPR for consideration at its annual Session. Step 5 Adoption at the Commission. The proposed draft standard is submitted through the Secretariat to the Executive Committee for critical review and to the Commission for review, with a view to its adoption as a Codex standard. The procedure for the elaboration of Codex standards for pesticide residue limits encompasses the recommended MRLs of JMPR on the basis of its risk assessment, MRL consideration and adoption at CCPR, and their adoption as Codex standards after the review at the Commission. Those MRLs that were not adopted at the Commission will be subject to consideration again.
个人分类: 法典专题|4140 次阅读|1 个评论
国际食品法典农药残留标准制定程序
wcwcsong 2010-6-28 17:13
国际食品法典农药残留标准制定程序 1 农药残留限量标准制定程序 CCPR 在农药残留限量标准制定过程中与 CAC 及 JMPR 保持密切关系,其制定过程为:首先 JMPR 根据 CCPR 制定的农药评估优先 列表 , 评估由成员国或公司提供的农药残留试验数据,提出 MRLs 建议值;然后 CCPR 按照法典标准制定程序,审议 JMPR 建议的 MRLs 值,最后提交 CAC 大会审议,审议通过后成为法典 MRLs 。标准几乎涉及所有种植、养殖农产品及其加工制品。 CCPR 制订农药法典 MRLs 的程序为一般程序和加速程序有两种。 1.1 一般程序 包括以下 8 个步骤, 第 1 步 确定标准制定计划,由农药评估优先列表特别工作组提出农药评估优先列表建议 ,然后由 CCPR 审议通过。第 2 步 评估,由 JMPR 专家组对农药残留进行风险评估,并提出建议, 包括推荐的 MRLs 、每日允许摄入量( ADIs ) 和 / 或急性参考剂量( ARfD )。 第 3 步 征求意见,首次征求各成员国和有关国际组织对 MRLs 建议标准草案的意见,包括建议标准草案可能对其经济利益的影响。第 4 步 CCPR 大会审议, CCPR 大会首次审议 MRLs 建议标准草案和反馈意见。第 5 步 CAC 大会审议,根据 CCPR 大会的结果, CAC 大会审议 MRLs 建议标准草案,通过后成为 MRLs 标准草案。第 6 步 再次征求意见,再次征求各成员国和有关国际组织对 MRLs 标准草案的意见,包括标准草案可能对其经济利益的影响。第 7 步 CCPR 大会再次审议, CCPR 大会再次审议 MRLs 标准草案和反馈意见。 第 8 步 CAC 大会审议,根据 CCPR 大会结果, CAC 大会审议 MRLs 标准草案,通过后成为法典 MRLs ,由 CAC 秘书处公布。 1.2 加速程序 在上述一般程序制定标准的 8 个步骤中省略第 6 和 7 步直接由第 4 步建议草案阶段进入第 5/8 步, CAC 大会审议通过后成为法典 MRLs ,由 CAC 秘书处公布。 应用加速程序制定 MRLs 必须满足以下条件,一是在第 3 步提出的新的 MRLs ;二是在 4 月份前能获得 JMPR 报告电子版;三是 JMPR 确认该农药没有膳食摄入问题;四是代表团对推进到第 5/8 步没有反对意见。 2 再残留限量 EMRLs 指由于环境背景值(包括以前农业应用,现已禁用的农药)而不是由于直接或间接使用农药而产生的农药残留,是食品、农畜产品中法定允许或认为可接受的农药最大残留量。制定 EMRLs 的目的是控制禁止使用后长久残留于环境的农药对食品、农畜产品的再次污染,以保护消费者健康和国际贸易。 EMRLs 是基于上述步骤,并根据有广泛地域代表性的残留监测数据(包括零残留结果)而不是根据残留试验数据制定的。最有可能制定 EMRLs 的是在环境中残留时间较长,有可能在食品或饲料残留并引起广泛关注的已禁止使用的农药。由于农药已禁用,对应的残留量逐渐降低, CCPR 将根据 JMPR 重新评估结果,每 5 年评价现有的 EMRLs 。
个人分类: 法典专题|5207 次阅读|0 个评论

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