Question and Answers on the regulation of GMOs in the EU

October 16, 2002

Brussels, 15 October 2002

This questions and answers fact sheet is divided into two sections; Part A covers legislation in force; Part B covers the legislative proposals on tracability and labelling put forward in July 2001

What are GMOs and GMMs?

Genetically modified organisms (GMOs) and genetically modified micro-organisms (GMMs) can be defined as organisms (and micro-organisms) in which the genetic material (DNA) has been altered in a way that does not occur naturally by mating or natural recombination. The technology is often called "modern biotechnology" or "gene technology", sometimes also "recombinant DNA technology" or "genetic engineering". It allows selected individual genes to be transferred from one organism into another, also between non-related species.

Part A: legislation in force

What is the current legislation in the EU on GMOs?

Community legislation on GMOs has been in place since the early 1990s and throughout the decade, this regulatory framework has been further extended and refined. The EU introduced specific legislation designed to protect its citizens' health and the environment while simultaneously creating a unified market for biotechnology.

The main legislation which authorises experimental releases and placing on the market of genetically modified organisms (GMOs) in the Community is Directive 90/220/EEC . This Directive will be repealed by the new, updated Directive 2001/18/EC of the European Parliament and Council on the deliberate release of genetically modified organisms on 17 October 2002.

Directive 2001/18/EC in general put in place a step-by-step approval process on a case by case assessment of the risks to human health and the environment before any GMO or product consisting of or containing GMOs, such as maize, tomatos, insects or microorganisms can be released into the environment or placed on the market.

Products derived from GMOs, such as paste or ketchup from a GMO tomato are not covered by this horizontal Directive but by vertical, sectoral legislation, for example the Regulation on Novel Foods and Novel Food Ingredients of January 1997(Regulation (EC) 258/97). Directive 90/219/EEC as amended by Council Directive 98/81/EC on the contained use of GMMs which regulates the contained use of GMMs for research and industrial purposes.

What has changed under the new Directive for the deliberate release of GMOs?

The revised Directive 2001/18/EC which repeals Directive 90/220/EEC on 17 October 2002, updates and strengthens the existing rules on the release of GMOs into the environment. In particular it introduces

  • a more detailed environmental risk assessment (see below);

  • mandatory monitoring requirements including long-term effects associated with the interaction with other GMOs and the environment;

  • mandatory information to the public;

  • general rules on mandatory labelling and traceability at all stages of the placing on the market;

  • first approvals for the release of GMOs to be limited to a maximum of ten years;

  • the consultation of the Scientific Committee(s) to be obligatory;

  • an obligation to consult the European Parliament on decisions to authorise the release of GMOs and

  • the possibility for Council of Ministers to adopt or reject a Commission proposal for authorisation of a GMO by qualified majority.
How does the environmental risk assessment procedure work from 17 October onwards?

The safety of GMOs depends on the characteristics of the inserted genetic material, the final organism that is produced the receiving environment and the interaction between the GMO and the environment. The objective of the environmental risk assessment is to identify and evaluate potential adverse effects of the GMO(s), either direct or indirect, immediate or delayed, taking also into account the cumulative and long term effects on human health and the environment which the deliberate release or the placing on the market of GMOs may have. The environmental risk assessment also looks specifically how the GM product was developed and examines the potential risks associated with the gene products in the product (for example toxic or allergenic proteins), and the possibility of a gene-transfer (for example of antibiotic resistance genes).

The methodology of the risk assessment is as follows:

  • Identification of any characteristics of the GMO(s) which may cause adverse effects

  • Evaluation of the potential consequences of each adverse effect

  • Evaluation of the likelihood of the occurrence of each identified potential adverse effect

  • Estimation of the risk posed by each identified characteristic of the GMO(s)

  • Application of management strategies for risks from the deliberate release or placing on the market of GMO(s)

  • Determination of the overall risk of the GMO(s)
The Scientific Committee on Plants (SCP) has issued opinions on 17 GM plants under Directive 90/220/EEC . In one case an unfavourable opinion was given due to an insufficient risk assessment of the presence of a number of uncharacterised genes and particularly the gene which confers resistance to amikacin, a clinically important antibiotic. This application was withdrawn.

The Scientific Committee on Food is responsible for opinions relating to Novel Foods. This Committee has issued 3 favourable opinion on food of plant origin (tomato and maize) and 4 on products of microbial origin.

What is the procedure for approval of the release of GMOs into the environment?

Under Directive 2001/18/EC , a company intending to market a GMO must first submit an application to the competent national authority of the Member State where the product is to be first placed on the market. For experimental releases, notifications are examined and consent is granted as appropriate by the authorities of the Member State in which the release is to be conducted.

The application must include a full environmental risk assessment for experimental releases and for placing on the market. If the national authority gives a favourable opinion on the placing on the market of the GMO concerned, this Member State informs the other Member States via the Commission. If there are no objections, the competent authority that carried out the original evaluation grants the consent for the placing on the market of the product. The product may then be placed on the market throughout the European Union in conformity with any conditions required in that consent.

If any objections are raised, a decision has to be taken at Community level. The Commission first asks for the opinion of its Scientific Committees composed of independent scientists, highly qualified in the fields associated with medicine, nutrition, toxicology, biology, chemistry, or other similar disciplines.

If the scientific opinion is favourable, the Commission then proposes a draft Decision to the Regulatory Committee composed of representatives of Member States for opinion. If the Regulatory Committee gives a favourable opinion, the Commission adopts the Decision.

If not, the draft Decision is submitted to the Council of Ministers for adoption by qualified majority or rejection. If the Council does not act within 3 months, the Commission can adopt the decision.

During the notification process he public will also be informed and has access to the publicly available data on the internet ( http://gmoinfo.jrc.it ) for example the summary notification format the assessment reports of the competent authorities or the opinion of the Scientific Committees.

How many GMOs have been approved for release into the environment?

Since Directive 90/220/EEC entered into force in October 1991, the commercial release of 18 GMOs has been authorised in the EU by a Commission Decision, mostly following a qualified majority vote in the Regulatory Committee. In two cases the Commission Decision has not yet been implemented by the Member State (see Annex 1).

Since October 1998 no further authorisations have been granted and there are currently 13 applications pending (see Annex 2). Some Member States have invoked Article 16, the so-called safeguard clause, of Directive 90/220/EEC to temporarily ban the placing on the market of genetically modified maize and oilseed rape products in their territories. There are currently nine ongoing Article 16 cases involving Austria, Luxembourg, France, Greece, Germany and United Kingdom. These cases have been examined by the Scientific Committee on Plants, which in all cases deemed that the information submitted by Member States did not justify their bans.What are the current rules on the marketing of GM foods?

Regulation (EC) 258/97 on Novel Foods and Novel Food Ingredients sets out rules for authorisation and labelling of novel foods including food products containing, consisting or produced from GMOs.

The first step of an authorisation procedure is an assessment of an application to market a GM food product by the Member State where the food is to be first placed on the market. In case of a favourable opinion, this Member State informs the other Member States via the Commission. If there are no objections against the application, this Member State can authorise the product for marketing in the entire EU.

If there are objections by other Member States, a decision at Community level is required. The Commission consults the Scientific Committees on matters relating to public health and adopts a decision after receiving a favourable opinion from the Regulatory Committee composed of Member State representatives. As a derogation from the full authorisation procedure, the Novel Foods Regulation provides for a simplified procedure for foods derived from GMOs but no longer containing GMOs which are "substantially equivalent" to existing foods with respect to composition, nutritional value, metabolism, intended use and the level of undesirable substances. In such cases, the companies only have to notify the Commission when placing a product on the market together with either scientific justification that the product is substantially equivalent or an opinion to the same effect, delivered by the competent authorities of a Member State.

How many GMOs have been approved for use in food products?

Two genetically modified plants, a variety of soybean and a variety of maize have been authorised under Directive 90/220/EEC prior to the entry into force of the Novel Foods Regulation, to be on the European market for the use in food. Under the Novel Foods Regulation no products consisting of or containing live GMOs have so far been authorised under the full procedure. Eleven applications concerning such products are pending at different stages in the procedure. (Annex 3) Several products produced from GMOs have been notified to the Commission as being substantially equivalent (see Annex 4). The list of notifications is published in the Official Journal of the EU once a year.

What are the current rules on genetically modified feed and which ones have been authorised?

There is currently no Community legislation governing the use of material derived from GMOs in feed. This is provided for in the Proposal on GM food and feed, which was adopted by the Commission on 25 July 2001. However, eight GMOs are authorised in accordance with Directive 90/220/EEC for the purpose of use in feed; these are four maize varieties, three rape varieties and one soya variety. (See Annex1)

What are the current rules on genetically modified seeds?

Community legislation on seeds, notably Directive 98/95/EC , specifies that national authorities that have agreed to the use of a seed on their territory must notify this acceptance to the Commission. The Commission examines the information supplied by the Member State concerned and its compliance with the provisions of Community seeds legislation. If such is the case, the Commission includes the variety concerned in the "Common Catalogue of varieties of Agricultural Plant Species" which means the seed can be marketed throughout the EU. The seed legislation furthermore requires that GMO seed varieties have to be authorised in accordance with Directive 90/220/EEC before they are included in the Common Catalogue and marketed in the EU. If the seed is intended for use in food, it also has to be authorised in accordance with the Novel Foods Regulation.

Legislation on the marketing of forestry reproductive material also requires prior authorisation of GM material in line with the requirements of Directive 90/220 . Community rules governing the marketing of vine material in line with Directive 90/220/EEC have also been adopted.

Further rules on growing conditions and other requirements for purity concerning the presence of GM seeds in seed lots of traditional varieties, as well as detailed labelling rules are to be proposed.

How many GM seeds have been authorised

So far only two GM seed varieties have been included in the Common Catalogue for seed varieties which can be marketed in the EU, after prior authorisation under Directive 90/220/EEC (chicory for industrial purposes, authorised to be marketed for breeding purposes only; See Annex 1). A further 18 applications for inclusion in the Common catalogue of GM seed varieties are currently pending (maize).

What are the rules for Medicines, Protection of workers and Transport

Authorisation of medicinal products for human and veterinary use (including such derived from genetically modified organisms) is regulated under Regulation (EEC) 2309/93 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use.

Council Directive 90/679/EEC on the protection of workers from the risks related to exposure to biological agents at work also regulates GMOs alongside other biological agents.

What are the current rules on labelling?

The EU recognises the consumers' right for information and labelling as a tool to make an informed choice.

Since 1997 labelling to indicate the presence of GMOs as such or in a product is mandatory. From 17 October 2002 onwards Directive 2001/18/EC foresees that Member States shall take all necessary measures to ensure a labelling of GMOs as or in products at all stages of the placing on the market.

The Novel Foods Regulation provides for the mandatory labelling of foods and food ingredients which contain or consist of a GMO without prejudice to the other labelling requirements of Community law. The labelling requirements for foods derived from GMO, but no longer containing GMO are more complicated and based on the concept of equivalence (1) .

Council Regulation 1139/98 lays down provisions for the labelling of foods and food ingredients derived from one maize and one soya (2) variety based on the presence of DNA or protein resulting from genetic modification. This criterion serves as a model providing the rules applicable to labelling of all foods and food ingredients derived from GMO.

In January 2000, the Commission adopted Regulation (EC) 50/2000 ensuring that also additives and flavourings have to be labelled if DNA or protein of GMO origin is present in the final product.

Regulation (EC) 49/2000 addresses the problem of adventitious contamination of GM material in conventional food. It introduces a 1% de minimis threshold for DNA or protein resulting from genetic modification below which labelling is not required, if operators can demonstrate that they have used appropriate steps to avoid the presence of GM material.

Genetically modified seed varieties must be labelled, in accordance with Council Directive 98/95/EEC . The label has to show clearly that it is a GM variety.

Currently, there is no specific Community legislation on the labelling of GMO feed. The general labelling rules under Directive 2001/18/EC apply from 17 October 2002. A new Novel Feed legislation will foresee provisions for labelling.

Part B: New legislative proposals

What are the contents of the latest proposals from European Commission concerning traceability and labelling of GMOs?

The European Commission adopted on 25 July 2001 two legislative proposals on GMOs. They set up a harmonised community system to trace GMOs, introduce the labelling of GM feed, reinforce the current labelling rules on GM food and establish a streamlined authorisation procedure for GMOs in food and feed and their deliberate release into the environment.

The proposals aim to put into place a stringent regulatory framework and to close existing legal gaps. They address the legitimate concerns of citizens, consumer organisations and economic operators.   A strict safety assessment of GMOs will continue to assure a high level of health and environmental protection. The labelling of all GM food and feed products will allow consumers and farmers to decide if they want to buy food or feed produced from a GMO, or not.

The package consists of:

Why is the Commission proposing specific rules on traceability of GMOs?

Traceability provides the means to trace products containing or produced from GMOs through the production and distribution chains. The general objectives are to facilitate:

  • control and verification of labelling claims

  • targeted monitoring of potential effects on the environment, where appropriate.

  • withdrawal of products that contain or consist of GMOs should an unforeseen risk to human health or the environment be established;
However, whilst Directive 2001/18 includes general provisions on which a traceability system for GMOs could be based, it neither contains a definition of traceability for GMOs, nor does it include the objectives of traceability or a complete approach for its implementation.

Differences and overlap between national laws, regulations and administrative provisions concerning traceability of GMOs and food and feed products produced from GMOs may hinder the free movement of products and create conditions of unfair competition. A Community Regulation based on the requirements of Directive 2001/18/EC and laying down a harmonised framework for traceability of such products would provide legal certainty and a coherent approach, and thus contribute to the effective functioning of the internal market.

Does traceability apply to GMOs and GM products only, or also to other food products?

Traceability for certain products has existed for many years. The proposed regulation sets specific traceability requirements for GM products. Traceability specifically for GMOs was introduced in general terms into Community legislation with Directive 2001/18/EC (3) which requires that Member States ensure traceability at all stages of the placing on the market for GMOs. (General traceability provisions have already been laid down in Community legislation concerning food, feed and seed. Legislation for specific traceability scheme for beef products has been put into place as in response to the BSE crisis (Regulation 1760/2000/EC ). Council and Parliament Regulation (Regulation EC/178/2002) laying down the general principles and requirements of food law, establishes also the principle of traceability at all stages of the production and distribution chain in the food and feed sectors.

What are the new rules on traceability of GMOs?

Under the rules of the proposed Regulation on traceability business operators must transmit and retain information about products that contain or are produced from GMOs at each stage of the placing on the market. In particular, the requirements are that:

  • operators shall have systems and procedures in place to identify to whom and from whom products are made available;

  • for GMOs intendedfor deliberate release into the environment , operators must transmit specified information on the identity of the individual GMO(s) a product contains;

  • for GMOs intendedfor food, feed or for processing , business operators may either transmit the specified information mentioned above or transmit a declaration that the product shall only be used as food or feed or for processing, together with the identity of the GMO(s) that the product may contain;

  • for food and feed produced from GMO(s) operators shall inform the next operator in the chain that the product is produced from GMO(s);

  • operators shall retain the information for a period of 5 years and make it available to competent authorities on demand.
Transmission and keeping records of this information will reduce the need for sampling and testing of products. To facilitate a co-ordinated approach for inspection and control by the Member States, the Commission will develop technical guidance on sampling and testing methods prior to the application of this proposed regulation.

How does traceability work in practice?

Traceability can be defined as the ability to trace products through all stages of the production and distribution line. Traceability starts with the company that develops a GMO, for instance a genetically modified seed. This company would then have to inform any purchaser of the seed that it is genetically modified, together with more specified information allowing the specific GMO to be precisely identified. The company is also obliged to keep a register of business operators who have bought the seed.

Equally the farmer would have to inform any purchaser of the harvest that it is genetically modified and keep a register of operators to whom he has made the harvest available.

The proposal covers all GMOs that have received Community authorisation for the placing on the market, that is all products, including food and feed, containing or consisting of GMOs. Examples are seeds, which have been genetically modified and bulk quantities or shipments of whole GM grain eg.soybean and maize.

The proposal also covers food and feed which are derived from a GMO. This includes tomato paste and ketchup produced from a GM tomato or starch, oil or flour produced from a GM maize.

What are the cost implications for operators of the traceability proposal?

It is difficult to estimate the exact costs of introducing traceability specifically for GMOs and products derived from GMOs.

Information with respect to the supplier, customer, price and transaction date as well as the nature, source, contents and amount of the product already accompanies the majority of transactions. This information has also to be retained by operators under national administrative systems, for example for filling in VAT returns. Transmission and retention of the information specified in the proposal could largely be incorporated into existing systems for transactions and as such, should not imply significant extra costs for operators.

What are the new proposed labelling rules and what is the difference with the existing rules?

The proposal extends the current labelling provisions to all genetically modified food or feed, irrespective of the detectability of genetically modified DNA or protein. All food and feed which consist of, contain or are produced from GMOs would have to be labelled as such. The purpose is to inform consumers and farmers about the exact nature and characteristics of the food or feed, so that they can make informed choices.

The current GM labelling system is based on the detectability of genetically modified DNA or protein in the final food product. In practice this means that highly processed foodstuffs produced from GM material, such as highly refined oils, do not need to be labelled. The proposed labelling rules extend the labelling requirements to all food and ingredients produced from GMOs to allow consumers to exercise their freedom of choice.

Genetically modified feed will need to be labelled along the same principles to give livestock farmers accurate information on the composition and properties of feed. This will mean that a large number of feedstuffs currently not subject to GM labelling requirements, such as GM soy meal in feed or compound feedstuffs and the four genetically modified feed plants authorised under Directive 90/220/EEC will in future need to be labelled. See also Annex 5.

Will the meat or milk of an animal fed with GM feed also be labelled as GM?

In line with the general EU rules on labelling, the proposal does not require labelling of products that are not food ingredients such as processing aids. It does not require labelling of products such as meat, milk or eggs obtained from animals fed with genetically modified feed or treated with genetically modified medicinal products.

See also Annex 5.

How will GM food and feed in future be authorised?

Clear rules are already set out in the EU for the assessment and authorisation of GMOs and GM-food, but the responsibilities are currently divided between the Member States and the Community. The Commission has proposed to replace this with a "one door one key" procedure for the scientific assessment and authorisation of GMOs and GM food and feed It puts in place a streamlined, uniform and transparent Community procedure for all marketing applications, whether they concern the GMO itself or the food and feed products derived thereof. This means that business operators need not request separate authorisations for use of the GMO, and for its use in feed or in food, but that a single risk assessment and a single authorisation are given for a GMO and its possible uses. This will ensure that experiences such as with Starlink maize in the US are avoided because GMOs likely to be used as food and feed can only be authorised for both uses, or not at all.

The scientific risk assessment will be carried out by the European Food Authority covering both the environmental risk and human and animal health safety assessment. Its opinion will be made available to the public and the public will have the possibility to make comments. On the basis of the opinion of the European Food Authority, the Commission will draft a proposal for granting or refusing authorisation. The proposal will, as it is currently the case, be approved through qualified majority of the Member States within a Regulatory Committee.

Products authorised shall be entered into a public register of GM-food and feed. Authorisations will be granted for a period of 10 years, subject where appropriate to a post-market monitoring plan. Authorisations are renewable for 10-year periods.

The simplified procedure for putting on the market GM-foods which are considered to be substantially equivalent to existing foods will be abandoned.

Will there be new rules on GM seed?

Two further proposals relating to GM seeds in seeds of conventional varieties are to be adopted in the near future. The first one is a Commission Directive amending the annexes of the different seed Directives, setting additional conditions and requirements concerning the adventitious or technically unavoidable presence of GM seeds in seed lots of non-GM varieties and specifying the labelling requirements of seeds of genetically modified varieties. 

At the same time a Commission Regulation on a protocol for sampling and testing of seed lots of non-GM varieties for the presence of GM seed will define how seed testing has to be carried out when applying the requirements set out in the previously mentioned Commission Directivewill be put forward.

Why is the Commission proposing to allow the presence of traces of non-approved GMOs?

The adventitious or unintended presence of GMOs in products placed on the market in the European Union is largely unavoidable and can occur during cultivation, handling, storage and transport. This situation already exists and affects products originating both in the Community and third countries.

This is not a problem which is not unique to GMOs. In the production of food, feed and seed, it is practically impossible to achieve products that are 100% pure.

The present proposal acknowledges this fact and defines the specific conditions under which a technically unavoidable presence of unauthorised GMOs could be permitted. A number of GMOs have already been assessed by the Scientific Committees advising the European Commission as not posing a danger to environment and health, but their final approval is still pending. The proposal allows the presence of these GMOs in a food or feed up to a maximum of 1% below which labelling and traceability will not be enforced. This is on the basis that the presence of such material is adventitious or technically unavoidable and has been subject to a scientific risk assessment by the relevant Scientific Committees or European Food Authority, which has concluded that the material does not present a risk for human health and the environment.

This exemption aims to solve the problem faced by operators who have tried to avoid GMOs, but find that their products contain a low percentage of GM material due to accidental or technically unavoidable contamination. Current legislation on GM foods (Regulation 1139/98 , see above) already sets a threshold of 1% for the labelling of approved GM material.

Are the new labelling rules in line with the international trade rules?

The proposals take account of the Community's international trade commitments and of the requirements of the Cartagena Protocol on Biosafety with respect to obligations of importers. A further legislative proposal setting rules concerning the obligations of exporters and other elements of the Cartagena Protocol is being prepared.

Will the Commission resume the authorisation process of GMOs?

The revised rules on the deliberate release of genetically modified organisms in Directive 2001/18/EC set out effective, efficient and transparent measures to ensure a high level of protection for human health and the environment. The two legislative proposals put forward in July 2001 build on the principles of this Directive and provide a regulatory framework for labelling and traceability. Together, this package of measures aims to address the concerns of Member States and to build consumer confidence in the authorisation of GM products. The revised Directive and the adoption of the two proposals for Regulations are expected to pave the way for a resumption of GM authorisations in the European Union.

How is the issue of exchange of GMOs regulated with Countries outside of the EU?

The UNEP Cartagena Protocol on Biosavety to the Convention on Biological Diversity was adopted on 29 January 2000. The overall purpose of this United Nations agreement is to establish common rules to be followed in transboundary movements of GMOs in order to ensure, on a global scale, the protection of biodiversity and of human health. The Commission Proposal on the transboundary movements of GMOs, dated from 18 February 2002, is linked to the recent ratification by the European Community of the Cartagena Protocol on Biosafety.

The European Union has to fulfil its international obligations and therefore we transpose into our own legal order the provisions of the Biosafety Protocol. The Commission's Proposal complements the existing Community regulatory framework, in particular for exports of GMOs, in order to align it with the provisions of the Biosafety Protocol.

The main elements of the proposal are the following:

  • Firstly, the obligation to notify exports of GMOs intended for deliberate release into the environment;

  • Secondly, the obligation to provide information to our international partners on Community practices, legislation and decisions on GMOs, as well as on accidental releases of GMOs;

  • Thirdly, a set of rules for identifying GMOs for exports. These rules are in line with latest developments in Community legislation on GMOs, and in particular with the provisions of the Draft Regulation on Traceability and Labelling.
The current Proposal does not foresee new specific Community provisions for imports or for movements of GMOs between Member States. These operations will continue to be covered by existing Community legislation.

Annex 1

GMO PRODUCTS APPROVED UNDER DIRECTIVE 90/220/EEC

ProductNotifierDate of Commission Decision (4) / Member State Consent (5) 1. Vaccine against Aujeszky's diseaseVemie Veterinär Chemie GmbH18.12.922. Vaccine against rabiesRhône-Mêrieux C/B/92/B28 & C/F/93/03-0219.10.933. Tobacco tolerant to bromoxynilSEITA C/F/93/08-0208.06.944. Vaccine against Aujeszky's disease (further uses) (6) Vemie Veterinär Chemie GmbH [Tables]

DN: MEMO/02/160 Date: 15/10/2002

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