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美国国务院批准转基因食品标签法

美国国务院批准转基因食品标签法

美国国务院批准转基因食品标签法
白小宁
【期刊名称】《农药科学与管理》
【年(卷),期】2014(35)8
【摘要】美国佛蒙特州的已成为第一个在国家批准的立法。

将需要从转基因作物派生的食品的标签。

佛蒙特州州长彼得·沙姆林签署法案成为法律,尽管由食品和转基因种子公司即将法律挑战的威胁。

【总页数】1页(P32-32)
【关键词】转基因食品;标签法;美国;国务院;转基因作物;种子公司;法律
【作者】白小宁
【作者单位】
【正文语种】中文
【中图分类】S572.032
【相关文献】
1.美国就转基因食品标签立法 [J], ;
2.美国国会通过首个转基因食品标签法案 [J], ;
3.美国就转基因食品标签立法 [J],
4.美国发布转基因食品标签最终法规 [J],
5.中华人民共和国商标法实施细则(一九八八年一月三日国务院批准修订,一九九三年七月十五日国务院批准第二次修订) [J],
因版权原因,仅展示原文概要,查看原文内容请购买。

日本转基因食品标识法

日本转基因食品标识法

日本《转基因食品标识法》的主要内容日本《转基因食品标识法》(以下简称“标识法”)对已经通过安全性认证的大豆、玉米、马铃薯、油菜籽、棉籽5种转基因农产品及以这些农产品为主要原料、加工后仍然残留重组DNA或由其编码的蛋白质的食品,制定了具体标识方法。

要点如下:(一)适用范围及定义“标识法”适用于对农产品和加工食品的管理。

“标识法”管理的农产品和相关术语的定义如下:指定农产品:包括大豆(含毛豆和黄豆芽)、玉米和马铃薯、油菜籽、棉籽,其中有一些作物品种是利用重组DNA技术开发的。

重组DNA技术:将DNA分离,然后使用酶等物质将其重新进行组合,并向具有繁殖能力的受体活细胞导入该重组DNA的一种技术方法。

转基因农产品:利用重组DNA技术得到的农产品。

非转基因农产品:属于指定农产品,但不是转基因产品。

区别性生产流通管理:是一种处理非转基因作物的方法,它通过对从海外农场到日本的生产、销售和加工的每一个阶段进行控制,避免混入转基因作物。

同时在农产品分离阶段都必须出具相关证明文件,以保证结论真实。

主要原料:在产品原料构成中比例排前三位,且重量是产品总重量5%以上的原料。

(二)标识方法“标识法”规定了指定农产品及其加工食品的具体标识方法。

第一,“加工食品”的标识方法。

以指定农产品为主要原料的加工食品(包括该食品的再加工食品)(参见表2左栏),如果食品中重组DNA或由其编码的蛋白质仍有残留,那么所有的食品生产者、制造商、包装商或进口商(或根据零售商与生产者、制造商和包装商达成的协议,对产品负有标识义务的零售商),除了要对《加工食品质量标识法》第4条所规定的项目进行标识外,还必须在食品标签上注明其主要原料(参见表2右栏)。

但食品容器或包装上可用于贴标签的空间小于30cm2的情况除外。

具体标识方法如下:(1)如果加工食品是以实行区别性生产流通管理的转基因农产品为主要原料,那么无需考虑《加工食品质量标识法》第3条第6款的规定,而应该在食品原料名称后,注明该食品是转基因食品。

美国转基因产品的管理模式

美国转基因产品的管理模式

美国转基因产品的管理模式
厉建萌;刘信;沈平;宋贵文;赵欣;徐俊锋
【期刊名称】《浙江农业科学》
【年(卷),期】2011(000)002
【摘要】从转基因管理机构及其责任、管理方式、管理依据等方面对美国的转基因管理状况进行了详细的分析阐述.美国转基因产品安全管理着重于上市前的安全评价,对安全评价的每一过程进行详细记录以增加其可追溯性,对销售中的转基因食品没有规定强制性标识法规.
【总页数】5页(P227-231)
【作者】厉建萌;刘信;沈平;宋贵文;赵欣;徐俊锋
【作者单位】农业部科技发展中心,北京,100125;农业部科技发展中心,北
京,100125;农业部科技发展中心,北京,100125;农业部科技发展中心,北京,100125;农业部科技发展中心,北京,100125;浙江省农业科学院,农产品质量标准研究所,浙江,杭州,310021
【正文语种】中文
【中图分类】Q943
【相关文献】
1.日本转基因产品溯源管理模式 [J], 汪小福;厉建萌;陈笑芸;徐俊锋;郑蔚然
2.我国转基因食品安全管理存在的主要问题——由美国转基因产品“黄金大米”引发的思考 [J], 李文瑛;徐谷波
3.“欧盟式”转基因标识法将加剧美国转基因农产品困境 [J],
4.北京奥瑞金中国首个转基因玉米种子产品将进入美国 [J], ;
5.中国首个转基因玉米种子产品将卖给美国 [J],
因版权原因,仅展示原文概要,查看原文内容请购买。

转基因食品的标签法规与消费者权益

转基因食品的标签法规与消费者权益

转基因食品的标签法规与消费者权益随着科技的不断发展,转基因技术在农业领域得到了广泛应用。

转基因食品作为一种新型食品,引发了公众对其安全性和食用价值的担忧。

为了保障消费者的权益和权威机构对转基因食品的监管,各国纷纷出台了转基因食品的标签法规。

本文将从法规内容、标签意义和消费者权益三个方面,探讨转基因食品的标签法规与消费者权益。

一、法规内容转基因食品的标签法规主要包括转基因食品的标签要求和标签的信息披露。

1. 标签要求转基因食品的标签应明确标示其属于转基因食品,遵循真实、准确和明了的原则,确保消费者能够充分了解食品的基本信息。

标签的字体应清晰可辨,与其他信息有明显区分。

同时,标签的位置应显眼,并不得以任何方式掩盖或混淆。

2. 标签的信息披露标签的信息披露是转基因食品标签的核心内容,主要包括以下几个方面:(1)转基因成分:标签应明确说明食品是否含有转基因成分,以及将转基因成分与非转基因成分区分。

(2)食品功能:标签应说明食品的功能,如增强免疫力、促进生长等,以便消费者根据自身需求选择合适的食品。

(3)食品安全性:标签应提供食品安全性相关信息,如经过安全评估、检测合格等。

(4)生产信息:标签应提供食品的生产企业、生产日期和有效期等信息,以便消费者了解食品的质量和来源。

二、标签意义转基因食品的标签具有重要的意义,以下是其主要意义:1. 保护消费者权益标签作为消费者获取信息的窗口,能够让消费者准确了解食品的成分和安全性,从而保护其权益。

消费者可以根据自身需求和健康状况,选择合适的食品,避免潜在的风险。

2. 促进市场竞争标签能够促进市场竞争,通过信息的透明度,鼓励企业提高产品质量和安全性,以争取更多消费者的选择。

同时,透明的标签也能够促进消费者对转基因食品的认知与了解,降低其对转基因食品的疑虑与恐惧。

3. 强化法规执行标签作为转基因食品法规执行的一环,能够监督企业按照法规要求进行标注和披露。

标签的存在使得食品监管机构和消费者能够更加方便地对食品进行抽检和追踪,确保食品市场的安全和有序。

从VEREGEN TM的商品说明书内容看FDA植物新药评审的思路与要求

从VEREGEN TM的商品说明书内容看FDA植物新药评审的思路与要求
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转基因标识

转基因标识

转基因标识的实际使用转基因标识是根据转基因生物安全管理相关法律法规对含有转基因成分的食品、饲料和其它相关产品进行的标示。

转基因标识符合法律赋予消费者知情权和选择权的要求,为消费者提供相关信息,并使消费者在知情的情况下做出自己的选择。

一些转基因食品在超市被贴上了醒目的标签,以方便市民选择。

标识的方法分为3种,以转基因大豆为例:转基因大豆在进口时应在外包装上注明“转基因大豆”;进口经加工为豆油后,应注明“转基因大豆加工品”;如果某面食的加工中使用了转基因豆油,但制成品中已检测不出转基因成分,仍要注明“本产品加工原料中含有转基因豆油,但本产品中已不含有转基因成分”。

根据对不同国家或地区转基因产品标识管理法规的比较分析,可将转基因产品标识制度分为两种主要类型:即自愿标识和强制性标识。

第一批实施标识管理的农业转基因生物目录一、大豆种子、大豆、大豆粉、大豆油、豆粕二、玉米种子、玉米、玉米油、玉米粉(含税号为11022000、11031300、11042300的玉米粉)三、油菜种子、油菜籽、油菜籽油、油菜籽粕四、棉花种子五、番茄种子、鲜番茄、番茄酱简介转基因生物(genetically modified organisms)的基因组经过了人工修饰。

因为获得转基因生物的技术方法与之前其它任何育种方法都不一样,转基因生物安全的争论和质疑自其诞生开始就一直没有停止。

相关国际组织(如FAO/WHO和OECD等)先后指定了转基因食物安全评价的指南,建议对转基因生物及其产品的身份进行标识、公开表明身份。

相关国家出台了针对性的法律法规,用于规范各国相关产品的研发、生产和商业化。

保护消费者知情权消费者往往是通过商品标签或说明书了解商品的。

如果标签的内容不客观,就无法真实地反映商品的内在品质。

如果在含有转基因食品的标签上没有标识转基因,则容易使消费者误认为该食品为非转基因食品。

此做法实际上剥夺了消费者的知情权。

保护消费者选择权消费者主要担心转基因生物对人体健康和生态环境可能存在不良影响,所以在销售此类商品时,必须对这类商品进行标识,保证消费者有权根据自己的意愿自由选择转基因商品。

香港转基因食物标签标注指引

香港转基因食物标签标注指引

基因改造食物自願標籤指引目的本指引載述了為基因改造食物加上標籤的基本原則,以便業界為消費者提供真確有用的資料。

引言2. 國際間正致力訂立一套公認的基因改造食物標籤制度,但現時食品法典委員會 (Codex Alimentarius Commission) 為此仍未達致共識,相信一套國際認可的標準亦不能在短期內制定。

雖然如此,有些國家已各自就基因改造食物標籤訂立要求。

為了加強消費者對基因改造食物的認識及作出知情選擇的能力,食物安全中心支持本地食物業界主動為基因改造食物設立自願標籤制度。

食物環境衞生署 ( 其後由食物安全中心負責 ) 為此成立了一個工作小組,成員包括食物業界、消費者委員會及有關政府部門的代表,負責制定有關指引。

3. 本指引純屬建議性質,而業內人士應積極採納這個由業界、消費者團體和政府部門代表共同制定的指引。

業界人士亦必須注意不可對食物作出虛假的說明,所有食物標籤均要符合《公眾衞生及市政條例》 ( 第 132 章 ) 第 61 條的規定。

[ 第 61 條的條文載於附錄。

] 本指引將因應科技的發展及國際間有關基因改造食物標籤制度的進展而作出修改。

基本原則4. 本指引包括以下之基本原則:5. 原則一:《公眾衞生及市政條例》 ( 第 132 章 ) 就本港的食物安全管制訂定條文。

該條例第 61 條規定,任何人士不得對其出售的食物給予,或在其為出售而展出的食物上展示對食物作出虛假說明的標籤。

此外,《食物及藥物 ( 成分組合及標籤 ) 規例》亦訂明,凡屬預先包裝食物,均須依照規定的方式加上標記及標籤。

6. 原則二:考慮到在收割、運送、加工和貯存的過程中,基因改造和非基因改造的農作物可能會不經意地混在一起,因此本指引把標籤個別食物配料的閾限值定於百分之五。

此閾限值反映現階段業界實際能達至的水平。

7. 原則三:在以下的情況下,若基因改造食物與原來品種有顯著分別時,則建議在食物標籤上另加說明:(a) 成分組合或營養價值方面與原來品種有顯著的分別;(b) 妨礙人體吸收營養的因子或毒性物質的含量與原來品種有顯著的分別;(c) 含有原來品種所沒有的致敏原;(d) 食物的擬定用途與原來品種有顯著的分別;或(e) 在源自植物的食物內加入動物基因。

转基因食品,何必怕亮出身份?

转基因食品,何必怕亮出身份?
签 的 费 用 仅 相 当 于 原 成 本 的 69 -%; 巴 西 含转基 因成分 ”的声明 , 消费者 而言, 对
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术 在生 产 中的应 用? 反对 加贴 标签 者认 择权 。就食 品而言,消 费者 除了要 了解 份 额 ,美 国 依 阿 华 州 的 天 然 产 品 公 司 生 为 :转 基 因技 术本 身安全 的不确 定性使 价格 外,还有权 了解食 品的品名 、营养 产非转基 因大 豆食品后 ,年销售额 上升 消 费 者 产 生 了 恐 惧 心 理 , 如 果 加 贴 标 签 成分 、卫生成 分 、卫生指 标 、安 全性 因 到 10 万美元 , 长 了3 0 有 机棉花 00 增 0% 无 疑就 是告诉 消 费者 不要 购 买该 产品 ,
应用 。但是,如 果一项技 术的应 用有可 食 品外包装上 的标签来实 现 。对于 转基 标签, 价格 将会进 一步上 涨;新鲜 的蔬 能会危及 人类 的生 命,任 何一个理性 的 因食 品, 由于其本 身具有 安全 的不确 定 菜若标明是 “ 无公 害”的,零售价格 高于
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BILL AS INTRODUCED H.1122013Page 1of 19VT LEG #284431v.2AH.1121Introduced by Representatives Webb of Shelburne,Bartholomew of Hartland,2Zagar of Barnard,Partridge of Windham,McCullough of 3Williston,Bissonnette of Winooski,Burke of Brattleboro,4Buxton of Tunbridge,Carr of Brandon,Cheney of Norwich,5Christie of Hartford,Cross of Winooski,Dakin of Chester,6Deen of Westminster,Devereux of Mount Holly,Donahue of 7Northfield,Donovan of Burlington,Ellis of Waterbury,8Emmons of Springfield,Frank of Underhill,French of 9Randolph,Head of South Burlington,Hooper of Montpelier,10Keenan of St.Albans City,Krowinski of Burlington,Lanpher 11of Vergennes,Lenes of Shelburne,Marek of Newfane,Martin 12of Springfield,Martin of Wolcott,Masland of Thetford,13McCarthy of St.Albans City,McCormack of Burlington,Miller 14of Shaftsbury,Mrowicki of Putney,Nuovo of Middlebury,15Pearson of Burlington,Peltz of Woodbury,Rachelson of 16Burlington,Ram of Burlington,Sharpe of Bristol,Spengler of 17Colchester,Stevens of Waterbury,Stuart of Brattleboro,Till of 18Jericho,Toleno of Brattleboro,Townsend of South Burlington,19Waite-Simpson of Essex,Wizowaty of Burlington,and 20Woodward of Johnson21BILL AS INTRODUCED H.1122013Page 2of 19VT LEG #284431v.2AReferred to Committee on 1Date:2Subject:Consumer affairs;food labeling;genetic engineering3Statement of purpose of bill as introduced:This bill proposes to provide that 4food is misbranded if it is entirely or partially produced with genetic 5engineering and it is not labeled as genetically engineered.6An act relating to the labeling of food produced with genetic engineering 7It is hereby enacted by the General Assembly of the State of Vermont:8Sec.1.FINDINGS9The General Assembly finds and declares that:10(1)U.S.federal law does not provide for the necessary and satisfactory 11regulation of the safety and labeling of food that contains genetically 12engineered ingredients,as evidenced by the following:13(A)U.S.federal labeling and food and drug laws do not require14manufacturers of food produced from genetically engineered ingredients to 15label such food as genetically engineered.16(B)As indicated by the testimony of Dr.Robert Merker,a U.S.Food17and Drug Administration (FDA)Consumer Safety Officer,the FDA does not 18have statutory authority to require labeling of foods produced with genetic 19engineering.20BILL AS INTRODUCED H.1122013Page 3of 19VT LEG #284431v.2A(C)The FDA has adopted a policy regarding the labeling of food1produced from genetic engineering based on a conclusion that these products 2are generally regarded as safe with no material difference from conventional 3products.The FDA does not require genetically engineered foods to be labeled 4as such.5(D)Instead of specifically regulating the safety and labeling of food6produced from genetic engineering,the FDA regulates genetically engineered 7foods in the same way it regulates foods developed by traditional plant 8breeding,but,according to Dr.James Maryanski,FDA biotechnology 9coordinator (1985−2008), the decision to regulate genetically engineered food 10in this manner was a political decision not based in science.11(E)Under its regulatory framework,the FDA does not test the safety12of genetically engineered foods independently.Instead,manufacturers submit 13safety research and studies,the majority of which the manufacturers finance or 14conduct.15(F)There is a lack of consensus regarding the validity of the research16or science surrounding genetically engineered foods,or both.The result is 17public uncertainty about the nutrition,health,safety,environmental impacts,18and the proliferation of genetic engineering technology that is not fully 19understood or proven to be safe.20BILL AS INTRODUCED H.1122013Page 4of 19VT LEG #284431v.2A(G)There have been no long-term studies in the United States that1examine the safety of human consumption of genetically engineered foods.2(2)Genetically engineered ingredients are increasingly present in foods 3available for human consumption,as evidenced by the fact that:4(A)an estimated 70to 80percent of the processed foods sold in the5United States have at least one genetically engineered ingredient;and6(B)according to the U.S.Department of Agriculture,in 2011,7genetically engineered soybeans accounted for 94percent of U.S.soybean 8acreage,genetically engineered corn accounted for 88percent of U.S.corn 9acreage,and genetically engineered sugar beets accounted for 95percent of 10U.S.sugar beet acreage.11(3)Genetically engineered foods have an effect on health,safety,12agriculture,and the environment,as evidenced by the following:13(A)Independent studies in laboratory animals indicate that the14ingestion of genetically engineered foods may lead to health problems such as 15gastrointestinal damage,liver and kidney damage,reproductive problems,16immune system interference,and allergic responses.17(B)Trends in commodity agricultural production practices are toward18monocultured crop production,which may result in genetic homogeneity,loss 19of biodiversity,and increased vulnerability of crops to pests,diseases,and20BILL AS INTRODUCED H.1122013Page 5of 19VT LEG #284431v.2Avariable climate conditions.Genetically engineered crops are one tool used in 1commodity agricultural production.2(C)Genetically engineered crops that include pesticides may3adversely affect populations of butterflies and other nontarget insects.4(D)Organic food certification,which is generally construed not to5include ingredients produced from genetic engineering,can be adversely 6affected by contamination from genetically engineered crops.7(E)Cross-pollination from genetically engineered crops may have an8adverse effect on wild plant species.9(F)The proliferation of patented genetically engineered crops10reduces the options of farmers who may want to save their own seed.11(4)Vermont and other states do have the authority to regulate the 12labeling of genetically engineered foods as evidenced by the following:13(A)Under the Tenth Amendment to the U.S.Constitution and the14U.S.Supreme Court’s ruling in Florida Lime &Avocado Growers,Inc.v.15Paul ,373U.S.132(1963),states may regulate the retail sale of food in the 16interest of consumers when such regulation does not conflict with federal law.17(B)Under Holk v.Snapple Beverage Co.,575F.3d 329(3d Cir.182009),the Federal Food,Drug,and Cosmetic Act and the FDA policy for 19labels using the word “natural”do not preempt states from regulating the use 20of the word “natural.”21BILL AS INTRODUCED H.1122013Page 6of 19VT LEG #284431v.2A(C)The Supreme Court,in Milavetz,Gallop &Milavetz v.United1States ,130S.Ct.1324(2010),reaffirmed the proposition,first expressed in 2Zauderer v.Office of Disciplinary Counsel ,471U.S.626(1985),that “an 3advertiser’s [First Amendment]rights are adequately protected as long as 4disclosure requirements are reasonably related to the State’s interest in 5preventing deception of consumers.”6(D)Under current First Amendment jurisprudence,expressed in7National Electric Manufacturers Assn.v.Sorrell ,272F.3d 104(2d Cir.2001),8states are free to compel the disclosure of factual commercial speech as long as 9the means employed by the State are rationally related to the State’s legitimate 10interest.11(E)The decision of the U.S.Court of Appeals for the Second Circuit12in International Dairy Foods Ass’n v.Amestoy ,92F.3d 67(2d Cir.1996),is 13limited expressly to cases in which a state disclosure requirement is supported 14by no interest other than gratification of consumer curiosity.15(5)For multiple personal,health,religious,and economic reasons,the 16citizens of Vermont desire,require,and necessitate that food produced from 17genetic engineering be labeled as such,as evidenced by the following:18(A)Public opinion polls conducted by the Center for Rural Studies at19the University of Vermont indicate that a large majority of Vermonters want 20foods produced with genetic engineering to be labeled as such.21BILL AS INTRODUCED H.1122013Page 7of 19VT LEG #284431v.2A(B)Given that 6V.S.A.§641(9)defines “genetically engineered1seed”as “seed produced using a variety of methods ed to modify 2genetically organisms or influence their growth and development by means 3that are not possible under natural conditions or processes,”labeling foods 4produced with genetic engineering as “natural,”“naturally made,”“naturally 5grown,”“all natural,”or other descriptors of similar substance is inherently 6misleading and poses a risk of confusing and deceiving consumers,and 7conflicts with the general perception that “natural”foods are not genetically 8engineered.9(C)Vermont citizens with certain religious beliefs object to10producing foods using genetic engineering because of objections to tampering 11with the genetic makeup of life forms and the rapid introduction and 12proliferation of genetically engineered organisms and,therefore,need food to 13be labeled as genetically engineered in order to conform to religious beliefs.14(D)Requiring that foods produced through genetic engineering be15labeled as such will create additional market opportunities for those producers 16who are not certified as organic and whose products are not produced from 17genetic engineering.Such additional market opportunities will contribute to 18the vibrant and diversified agricultural community of Vermont.19(E)Labeling gives consumers information they can use to make20informed decisions about what products they would prefer to purchase.21BILL AS INTRODUCED H.1122013Page 8of 19VT LEG #284431v.2A(F)On March 12,2012,the Vermont Congressional Delegation,1along with 52other members of Congress,sent a letter to the Honorable 2Margaret Hamburg,Commissioner of the FDA,asking that the FDA require 3labeling of food produced with genetic engineering.4(6)Because both the FDA and the U.S.Congress have failed to require 5the labeling of food produced with genetic engineering,the State should 6exercise its authority to require food produced with genetic engineering to be 7labeled as such in order to serve the legitimate interests of the State to prevent 8inadvertent consumer deception,promote food safety,respect religious beliefs,9protect the environment,and promote economic development.10Sec.2.18V.S.A.chapter 82,subchapter 3is added to read:11Subchapter beling of Food Produced with12Genetic Engineering13§4091.PURPOSE14It is the purpose of this chapter to:15(1)Consumer confusion and deception.Reduce consumer confusion 16and deception and promote the disclosure of factual information on food labels 17to allow consumers to make informed decisions.18(2)Food safety.Promote food safety by allowing consumers to make 19informed dietary decisions when purchasing food,since genetically engineered 20food is considered to be recognized generally as safe by the U.S.Food and21BILL AS INTRODUCED H.1122013Page 9of 19VT LEG #284431v.2ADrug Administration despite a lack of consensus about that fact in the 1scientific community,and since scientific evidence indicates that foods 2produced using genetic engineering pose potential food safety and health 3issues related to allergenicity,antibiotic resistance,immune response,4reproductive problems,and liver and kidney damage.5(3)Protecting religious and cultural practice.Provide consumers with 6data from which they may make informed decisions for personal,religious,7moral,cultural,or ethical reasons.8(4)Environmental impacts.Assist consumers in making informed 9decisions about food purchases that have potential effects on the environment,10including:11(A)displacement of native flora and fauna;12(B)transfer of unnatural deoxyribonucleic acid to wild relatives and13organic crops;14(C)creation of herbicide-resistant “super weeds”and15pesticide-resistant insects;and16(D)ecosystem disruptions such as loss of biodiversity,increased17herbicide and pesticide use,and adverse effects on nontarget insects such as 18butterflies.19(5)Promoting economic development.Create additional market 20opportunities for those producers who are not certified organic and whose21BILL AS INTRODUCED H.1122013Page 10of 19VT LEG #284431v.2Aproducts are not produced using genetic engineering and allow consumers to 1make informed purchasing decisions.2§4092.DEFINITIONS 3As used in this subchapter:4(1)“Enzyme”means a protein that catalyzes chemical reactions of other 5substances without itself being destroyed or altered upon completion of the 6reactions.7(2)“Genetic engineering”means a food or food ingredient that is 8produced from an organism or organisms in which the genetic material has 9been changed through the application of:10(A)in vitro nucleic acid techniques,including recombinant11deoxyribonucleic acid (DNA)techniques and the direct injection of nucleic 12acid into cells or organelles;or13(B)fusion of cells (including protoplast fusion)or hybridization14techniques that overcome natural physiological,reproductive,or recombination 15barriers,where the donor cells or protoplasts do not fall within the same 16taxonomic group,in a way that does not occur by natural multiplication or 17natural recombination.18(3)“In vitro nucleic acid techniques”means techniques,including 19recombinant DNA or ribonucleic acid techniques,that use vector systems and 20techniques involving the direct introduction into the organisms of hereditary21BILL AS INTRODUCED H.1122013Page 11of 19VT LEG #284431v.2Amaterials prepared outside the organisms such as micro-injection,1chemoporation,electroporation,micro-encapsulation,and liposome fusion.2(4)“Organism”means any biological entity capable of replication,3reproduction,or transferring of genetic material.4(5)“Processed food”means any food other than a raw agricultural 5commodity and includes any food produced from a raw agricultural 6commodity that has been subjected to processing such as canning,smoking,7pressing,cooking,freezing,dehydration,fermentation,or milling.8(6)“Processing aid”means:9(A)a substance that is added to a food during the processing of the10food but that is removed in some manner from the food before the food is 11packaged in its finished form;12(B)a substance that is added to a food during processing,is13converted into constituents normally present in the food,and does not 14significantly increase the amount of the constituents naturally found in the 15food;or16(C)a substance that is added to a food for its technical or functional17effect in the processing but is present in the finished food at levels that do not 18have any technical or functional effect in that finished food.19BILL AS INTRODUCED H.1122013Page 12of 19VT LEG #284431v.2A(7)“Raw agricultural commodity”means any food in its raw or natural 1state.It includes any fruit that is washed,colored,or otherwise treated in its 2unpeeled natural form prior to marketing.3§BELING OF FOOD PRODUCED WITH GENETIC4ENGINEERING5(a)Except as set forth in section 4094of this title,food shall be labeled as 6produced entirely or in part from genetic engineering if it is a product:7(1)offered for retail sale in Vermont;and8(2)entirely or partially produced with genetic engineering.9(b)If a food is required to be labeled under subsection (a)of this section,it 10shall be labeled as follows:11(1)in the case of a raw agricultural commodity,on the package offered 12for retail sale,with the clear and conspicuous words,“produced from genetic 13engineering”on the front of the package of the commodity or in the case of 14any such commodity that is not separately packaged or labeled,on a label 15appearing on the retail store shelf or bin in which the commodity is displayed 16for sale;or17(2)in the case of any processed food,in clear and conspicuous language 18on the front or back of the package of the food,with the words “partially 19produced with genetic engineering”or “may be partially produced with genetic 20engineering.”21BILL AS INTRODUCED H.1122013Page 13of 19VT LEG #284431v.2A(c)Except as set forth under section 4094of this title,a food produced 1entirely or in part from genetic engineering shall not be labeled on the product,2in signage,or in advertising as “natural,”“naturally made,”“naturally grown,”3“all natural,”or any words of similar import that would have a tendency to 4mislead a consumer.5§4094.EXEMPTIONS6The following foods shall not be subject to the labeling requirements of 7section 4093of this title:8(1)Food consisting entirely of or derived entirely from an animal which 9has not itself been produced with genetic engineering,regardless of whether 10the animal has been fed or injected with any food or drug produced with 11genetic engineering.12(2)A raw agricultural commodity or food derived from it that has been 13grown,raised,or produced without the knowing and intentional use of food or 14seed produced with genetic engineering.Food will be deemed to be as 15described in this subdivision only if the person otherwise responsible for 16complying with the requirements of subsection 4093(a)of this title with 17respect to a raw agricultural commodity or food obtains,from whomever sold 18the commodity or food to that person,a sworn statement that the commodity or 19food has not been knowingly or intentionally produced with genetic 20engineering and has been segregated from and has not been knowingly or21BILL AS INTRODUCED H.1122013Page 14of 19VT LEG #284431v.2Aintentionally commingled with food that may have been produced with genetic 1engineering at any time.In providing such a sworn statement,any person may 2rely on a sworn statement from his or her own supplier that contains the 3affirmation set forth in this subdivision.4(3)Any processed food which would be subject to subsection 4093(a)of 5this title solely because it includes one or more processing aids or enzymes 6produced with genetic engineering.7(4)Any beverage that is subject to the provisions of Title 7.8(5)Until July 1,2019,any processed food that would be subject to 9subsection 4093(a)of this title solely because it includes one or more 10ingredients that have been produced with genetic engineering,provided that:11(A)no single such ingredient accounts for more than one-half of 0.912percent of the total weight of the processed food;and13(B)the processed food does not contain more than ten such14ingredients.15(6)Food that an independent organization has determined has not been 16knowingly and intentionally produced from or commingled with food or seed 17produced with genetic engineering,provided that the determination has been 18made pursuant to a sampling and testing procedure approved in regulations 19adopted by the Department.No sampling procedure shall be approved by the 20Department unless sampling is done according to a statistically valid sampling21BILL AS INTRODUCED H.1122013Page 15of 19VT LEG #284431v.2Aplan consistent with principles recommended by internationally recognized 1sources such as the International Standards Organization or the Grant and Feed 2Trade Association.No testing procedure shall be approved by the Department 3unless:4(A)it is consistent with the most recent “Guidelines on Performance5Criteria and Validation of Methods for Detection,Identification and 6Quantification of Specific DNA Sequences and Specific Proteins in Foods”7(CAC/GL 74(2010)),published by the Codex Alimentarius Commission;and8(B)it does not rely on testing of processed foods in which no DNA is9detectable.10(7)Food that has been lawfully certified to be labeled,marketed,and 11offered for sale as “organic”pursuant to the federal Organic Food Products Act 12of 1990and the regulations promulgated pursuant thereto by the U.S.13Department of Agriculture.14(8)Food that is not packaged for retail sale and that either:15(A)is a processed food prepared and intended for immediate human16consumption;or17(B)is served,sold,or otherwise provided in any restaurant or other18food establishment,as defined in section 4301of this title,that is primarily 19engaged in the sale of food prepared and intended for immediate human 20consumption.21BILL AS INTRODUCED H.1122013Page 16of 19VT LEG #284431v.2A(9)Medical food,as that term is defined in 21U.S.C.§360ee(b)(3).1§4095.SEVERABILITY2If any provision of this subchapter or its application to any person or 3circumstance is held invalid or in violation of the Constitution or laws of the 4United States or in violation of the Constitution or laws of Vermont,the 5invalidity or the violation shall not affect other provisions of this section which 6can be given effect without the invalid provision or application,and to this end,7the provisions of this section are severable.8§4096.PENALTIES9A person who violates the requirements of this subchapter shall be subject 10to penalty under section 4054of this title.Notwithstanding any other 11provision of law to the contrary,no violation of this subchapter shall give rise 12to any cause of action under 9V.S.A.chapter 63.13Sec.3.18V.S.A.§4051is amended to read:14§4051.DEFINITIONS15For the purposes of this chapter:16***17(2)The term “board”means the state board of health.“Commissioner”18means the Commissioner of Health.19***20BILL AS INTRODUCED H.1122013Page 17of 19VT LEG #284431v.2ASec.4.18V.S.A.§4053is amended to read:1§4053.REGULATIONS AND HEARINGS2(a)The authority to enforce this chapter is vested in the board3Commissioner.The board Commissioner shall from time to time for the 4efficient enforcement of this chapter promulgate adopt regulations after public 5hearing following due notice at least ten days in advance of the hearings to 6interested persons consistent with 3V.S.A.chapter 25.7(b)In addition to the other remedies provided in this chapter,the board 8Commissioner is hereby authorized through the attorney general Attorney 9General or state’s attorneys to apply to the civil or criminal division of any 10superior court,and the court shall have jurisdiction upon hearing and for cause 11shown,to grant a temporary or permanent injunction restraining any person 12from violating any provision of this chapter,irrespective of whether or not 13there exists an adequate remedy at law.14***15(d)Before any violation of this chapter is reported for institution of a 16criminal proceeding,the person against whom such proceeding is17contemplated may be given appropriate notice and an opportunity to present 18his or her views to the board Commissioner,either orally or in writing,with 19regard to the contemplated proceeding.Nothing in this chapter shall be 20construed as requiring the board Commissioner to report for prosecution or for21BILL AS INTRODUCED H.1122013Page 18of 19VT LEG #284431v.2Athe institution of libel proceedings minor violations of the chapter whenever he 1or she believes that the public interest will be best served by a suitable notice 2of warning in writing.3Sec.5.18V.S.A.§4060is amended to read:4§4060.MISBRANDED FOOD5A food shall be deemed to be misbranded:6***7(13)If it is labeled in violation of section 4093of this title.8Sec.6.18V.S.A.§4069is amended to read:9§4069.REGULATIONS;AUTHORITY10(a)The authority to promulgate adopt regulations for the efficient 11enforcement of this chapter is hereby vested in the board Commissioner.The 12board Commissioner may make the regulations promulgated adopted under 13this chapter conform,insofar as practicable,with those promulgated under the 14federal act;.15(b)Hearings authorized or required by this chapter shall be conducted by 16the board Commissioner or such officer,agent,or employee as the board 17Commissioner may designate for the purpose;.18(c)Before promulgating adopting any regulations contemplated by section 194058;4060(10);4061;4064(d),(f),(g),(h),and (k);or 4068(b)of this title,the 20board Commissioner shall give appropriate notice of the proposal and of the21BILL AS INTRODUCED H.1122013Page 19of 19VT LEG #284431v.2Atime and place for a hearing.The regulation so promulgated adopted shall 1become effective on a date fixed by the board Commissioner,which date shall 2not be earlier than 60days after its promulgation adoption.The regulation 3may be amended or repealed in the same manner as is provided for its 4adoption,except that in the case of a regulation amending or repealing any 5such regulation,the board Commissioner,to such the extent as it deems 6necessary in order to prevent undue hardship,may disregard the foregoing 7provisions regarding notice,hearing,or effective date.8Sec.7.STATUTORY REVISION9In its statutory revision capacity under 2V.S.A.§424,the Office of 10Legislative Council shall,where appropriate,replace the term “Board of 11Health”in 18V.S.A chapter 82wherever it appears with the terms 12“Commissioner of Health”or “Commissioner.”13Sec.8.EFFECTIVE DATE14This act shall take effect on July 1,2014.15。

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