Difference between revisions of "Team:Glasgow/GMOLegislation"

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The Idea
 
The Idea
 
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As we are planning to make a food product containing genetically modified organisms (GMOs), we have investigated the current legislation regarding GMOs in food. The European Union has established rules to regulate the safety, authorisation, supervision and labeling of GMOs, which applies to food and animal feed1. This legislation aims to protect both human and animal health as well as the environment through high standard safety and risk assessments before a GMO can be placed on the market. In addition, a clear label must be placed on all GMO products, and traceability of all GMOs must be possible.
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To apply for authorisation, a single application that covers all uses (food, animal feed and cultivation) must be completed. Within two weeks of the application being sent in, the competent authority in the relevant EU country informs the European Food and Safety Authority (EFSA), who then has six months to process the application2. The EFSA panel is made up of scientists from across Europe with expertise in food and feed safety, environmental risk, and molecular characterisation and plant science.
 +
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The European Commission is then responsible for the risk management of the GMO. Based on EFSA’s assessment of the application, the Commission drafts a recommendation to either accept or reject the application2. The proposal is then sent to the Standing Committee on the Food Chain and Animal Health. If the Committee accepts the proposal, the Commission adopts it. If the application is rejected, the Council of the EU assesses the draft decision and decides if the Commission should adopt it or not. GMOs are only authorised if they are considered safe for human and animal health, as well as the environment2.
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There are very strict rules on the labeling of GMOs. The list of ingredients must clearly say either “genetically modified” or “produced from genetically modified [name of organism]”2. If the product contains no packaging, then this label must be placed in close proximity of it, for example in a note on the supermarket shelf where the product is kept. However, if the product contains less than 0.9% GMOs, it does not need to be labeled2.
  
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PICTURE
  
Vestibulum quis felis vel sapien iaculis ultricies vitae at tellus. Vestibulum nec risus sapien. Phasellus at euismod elit, at lobortis tortor. In non eros sodales, ultricies sem in, tempor urna. Phasellus non nibh eget nibh pulvinar faucibus. Vestibulum nec consequat nibh, nec hendrerit ante. Sed nulla elit, convallis quis metus non, interdum interdum purus. In ac lectus ligula. Praesent vestibulum tincidunt posuere. Vestibulum congue enim eget ligula consequat consequat. Nullam venenatis viverra purus, ac ullamcorper nunc maximus a. Quisque ipsum dolor, ultrices sit amet quam nec, lacinia sagittis sem. Vivamus maximus massa a urna porta viverra. Duis ornare nunc mauris. Praesent accumsan lectus a ante ullamcorper semper.
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The risk management is posed on a case-by-case basis. To get our product on the market, we would need to submit an application where we specify the type of food and describe in detail the method of production and manufacturing. In addition, we would need to state why we want to place our product on the market and that it would not raise any ethical or religious concerns from those consuming it. Since our product is aimed for human consumption, we would need to provide a way for post-marketing monitoring of our yogurt3.
 +
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The EU has a register of all authorized GMOs. It can be searched for products containing certain GMOs. The categories that have been registered are cotton, maize, oilseed rape, soybean, sugar beet and swede-rape4. Although, to date, no yogurt products have been found to contain GMOs, The Wall Street Journal reported that a Greek yogurt brand named Chobani has been using milk from cows that have been fed crops that have been genetically modified, such as soybean and corn5.
 +
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Some food products are not GMOs themselves, but include a GMO in it, such as tofu, which can contain modified soy to resist herbicides. Some products on the other hand are GMOs themselves, such as corn. Our product, yogurt, will be mainly made from milk, but it would contain living organisms that have been engineered to produce beta-carotene so it would lie somewhere in the middle of that spectrum. As our yogurt contains material produced by a GMO as well as the GMO itself, we would have to successfully pass the EU criteria for GMO food as explained above to place it on the market. Our product would have to pass the GM Food and Feed Regulation (EC 1829/2003) and EFSA would then make a decision in the next six months after making our application. We understand that GMO approval is a very long process; the arsenic biosensor that started off as Edinburgh’s iGEM project in 2006 are still waiting on their EU approval.
 +
 +
GMO legislation is not the same in other parts of the world. For example, the US approach assumes that regulation should “focus on the nature of the products, rather than the process in which they were produced”6. Plant GMOs are regulated under the Plant Protection Act, GMOs in food, drugs and biological products are regulated by the FDA (Food and Drug Administration), and GMO pesticides and microorganisms are regulated by the EPA (Environmental Protection Agency). The rules on GMOs in food supply are more lenient in the US. The FDA treats foods derived from GMOs like those derived from conventionally bred plants, and are “generally recognized as safe”6. However, premarket approval is required if the GMO product differs significantly in structure, function or composition from substances that are currently in food6. In our case, we would hypothesise that since we are using bacteria already present in yogurt and introduce beta-carotene (which safety is already well-characterised), our product would not require premarket approval. Although, the processes to ensure the level of beta-carotene produced stays below toxic limits will have to be clearly established and robust, and may require assessment. However, it could also be that the FDA takes the view that we intend to use our product to treat illnesses, which could then mean that it becomes a drug, requiring specific approval beyond its GMO status.
 +
 +
One of our target countries, India, used to be hostile to GMO testing. However, in the past year, eight Indian states have approved GM crop testing7. This still leaves more than 20 states and territories where field trials are not permitted. Cotton is India’s only permitted GM crop7. This slow progress might be detrimental to our potential product, as our idea permits people to make their own yogurt using genetically modified bacteria, but it could be more accepted in the future, especially given the use of our SIM device to prevent release.
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<ol class="references">
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<li>Eur-Lex, 2015. Genetically Modified Food and Feed. Accessed 25/09/2016 at <http://eur-lex.europa.eu/legal-content/EN/TXT/?uri=URISERV%3Al21154>.</li>
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<li>European Commission, 2016. Genetically Modified Organisms. Accessed 25/09/2016 at <http://ec.europa.eu/food/plant/gmo/index_en.htm>.</li>
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<li>Library of Congress, 2015. Restrictions on Genetically Modified Organisms: European Union. Accessed 15/10/16 at < https://www.loc.gov/law/help/restrictions-on-gmos/eu.php#Foodstuffs>.</li>
 +
<li>European Commission. EU Register of authorized GMOs. Accessed 15/10/16 at <http://ec.europa.eu/food/dyna/gm_register/index_en.cfm>.</li>
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<li>Gasparro A. and Josephs L. 2013. Whole Foods to Stop Selling Chobani Yogurt. Accessed 15/10/16 at <http://www.wsj.com/news/articles/SB10001424052702304367204579266201175528672>.</li>
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<li>Library of Congress, 2015. Restrictions on Genetically Modified Organisms: United States. Accessed 15/10/16 at <https://www.loc.gov/law/help/restrictions-on-gmos/usa.php>.</li>
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<li>Nature News, 2015. India eases stance on GM crop trials. Accessed 15/10/16 at < http://www.nature.com/news/india-eases-stance-on-gm-crop-trials-1.17529>.</li>
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</ol>
  
Vestibulum sodales tortor quis augue bibendum porttitor. Nam id est est. Proin congue, tellus vitae porta hendrerit, nisi leo viverra orci, ac euismod libero massa eu ante. Proin sit amet eleifend nisi. Ut congue turpis efficitur, porta metus fringilla, dignissim eros. Etiam rhoncus, libero quis lacinia hendrerit, metus nisi faucibus enim, vitae pretium lacus sem non mi. Pellentesque quis convallis turpis, nec porttitor mi. Vivamus in dictum sem. Etiam ac tempor ex. Cras quis porttitor nisi.
 
 
Donec lacinia odio in nisl dignissim dignissim. Curabitur cursus hendrerit aliquam. Vestibulum mollis mauris in diam mattis eleifend et sit amet nisi. Nam sed ipsum sed justo ornare volutpat. Etiam quis purus posuere, commodo nisl auctor, efficitur magna. Duis sed imperdiet est. Donec eget cursus justo. Donec blandit est elit, id porttitor diam eleifend in. Fusce condimentum sollicitudin fringilla. Nunc vel sapien dignissim, posuere nibh et, maximus lorem. Suspendisse potenti. Integer a dapibus mauris. Quisque id sagittis nibh, iaculis hendrerit felis. Aenean urna magna, ornare non lorem sit amet, pharetra suscipit augue. Sed sit amet sodales sapien.
 
 
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Revision as of 18:28, 17 October 2016

Glasgow iGEM 2016
GMO Legislation
Getting our product on the market
The Idea
As we are planning to make a food product containing genetically modified organisms (GMOs), we have investigated the current legislation regarding GMOs in food. The European Union has established rules to regulate the safety, authorisation, supervision and labeling of GMOs, which applies to food and animal feed1. This legislation aims to protect both human and animal health as well as the environment through high standard safety and risk assessments before a GMO can be placed on the market. In addition, a clear label must be placed on all GMO products, and traceability of all GMOs must be possible. To apply for authorisation, a single application that covers all uses (food, animal feed and cultivation) must be completed. Within two weeks of the application being sent in, the competent authority in the relevant EU country informs the European Food and Safety Authority (EFSA), who then has six months to process the application2. The EFSA panel is made up of scientists from across Europe with expertise in food and feed safety, environmental risk, and molecular characterisation and plant science. The European Commission is then responsible for the risk management of the GMO. Based on EFSA’s assessment of the application, the Commission drafts a recommendation to either accept or reject the application2. The proposal is then sent to the Standing Committee on the Food Chain and Animal Health. If the Committee accepts the proposal, the Commission adopts it. If the application is rejected, the Council of the EU assesses the draft decision and decides if the Commission should adopt it or not. GMOs are only authorised if they are considered safe for human and animal health, as well as the environment2. There are very strict rules on the labeling of GMOs. The list of ingredients must clearly say either “genetically modified” or “produced from genetically modified [name of organism]”2. If the product contains no packaging, then this label must be placed in close proximity of it, for example in a note on the supermarket shelf where the product is kept. However, if the product contains less than 0.9% GMOs, it does not need to be labeled2. PICTURE The risk management is posed on a case-by-case basis. To get our product on the market, we would need to submit an application where we specify the type of food and describe in detail the method of production and manufacturing. In addition, we would need to state why we want to place our product on the market and that it would not raise any ethical or religious concerns from those consuming it. Since our product is aimed for human consumption, we would need to provide a way for post-marketing monitoring of our yogurt3. The EU has a register of all authorized GMOs. It can be searched for products containing certain GMOs. The categories that have been registered are cotton, maize, oilseed rape, soybean, sugar beet and swede-rape4. Although, to date, no yogurt products have been found to contain GMOs, The Wall Street Journal reported that a Greek yogurt brand named Chobani has been using milk from cows that have been fed crops that have been genetically modified, such as soybean and corn5. Some food products are not GMOs themselves, but include a GMO in it, such as tofu, which can contain modified soy to resist herbicides. Some products on the other hand are GMOs themselves, such as corn. Our product, yogurt, will be mainly made from milk, but it would contain living organisms that have been engineered to produce beta-carotene so it would lie somewhere in the middle of that spectrum. As our yogurt contains material produced by a GMO as well as the GMO itself, we would have to successfully pass the EU criteria for GMO food as explained above to place it on the market. Our product would have to pass the GM Food and Feed Regulation (EC 1829/2003) and EFSA would then make a decision in the next six months after making our application. We understand that GMO approval is a very long process; the arsenic biosensor that started off as Edinburgh’s iGEM project in 2006 are still waiting on their EU approval. GMO legislation is not the same in other parts of the world. For example, the US approach assumes that regulation should “focus on the nature of the products, rather than the process in which they were produced”6. Plant GMOs are regulated under the Plant Protection Act, GMOs in food, drugs and biological products are regulated by the FDA (Food and Drug Administration), and GMO pesticides and microorganisms are regulated by the EPA (Environmental Protection Agency). The rules on GMOs in food supply are more lenient in the US. The FDA treats foods derived from GMOs like those derived from conventionally bred plants, and are “generally recognized as safe”6. However, premarket approval is required if the GMO product differs significantly in structure, function or composition from substances that are currently in food6. In our case, we would hypothesise that since we are using bacteria already present in yogurt and introduce beta-carotene (which safety is already well-characterised), our product would not require premarket approval. Although, the processes to ensure the level of beta-carotene produced stays below toxic limits will have to be clearly established and robust, and may require assessment. However, it could also be that the FDA takes the view that we intend to use our product to treat illnesses, which could then mean that it becomes a drug, requiring specific approval beyond its GMO status. One of our target countries, India, used to be hostile to GMO testing. However, in the past year, eight Indian states have approved GM crop testing7. This still leaves more than 20 states and territories where field trials are not permitted. Cotton is India’s only permitted GM crop7. This slow progress might be detrimental to our potential product, as our idea permits people to make their own yogurt using genetically modified bacteria, but it could be more accepted in the future, especially given the use of our SIM device to prevent release.
  1. Eur-Lex, 2015. Genetically Modified Food and Feed. Accessed 25/09/2016 at .
  2. European Commission, 2016. Genetically Modified Organisms. Accessed 25/09/2016 at .
  3. Library of Congress, 2015. Restrictions on Genetically Modified Organisms: European Union. Accessed 15/10/16 at < https://www.loc.gov/law/help/restrictions-on-gmos/eu.php#Foodstuffs>.
  4. European Commission. EU Register of authorized GMOs. Accessed 15/10/16 at .
  5. Gasparro A. and Josephs L. 2013. Whole Foods to Stop Selling Chobani Yogurt. Accessed 15/10/16 at .
  6. Library of Congress, 2015. Restrictions on Genetically Modified Organisms: United States. Accessed 15/10/16 at .
  7. Nature News, 2015. India eases stance on GM crop trials. Accessed 15/10/16 at < http://www.nature.com/news/india-eases-stance-on-gm-crop-trials-1.17529>.