GMO labelling and public consultation is made compulsory. The European Commission is obliged to consult the competent scientific committees on any question affecting human health or the environment.

Registers must be established for the purpose of recording information on genetic modifications in GMOs alongside their location. Rules on the operation of these registers are laid down in Decision 2004/204/EC.

The Commission must publish a report on the experience of GMOs placed on the market and a summary of the measures taken by EU countries to implement this directive every 3 years.

Although this directive allows EU countries to restrict or prohibit the release of GMOs that constitute a risk to human health and the environment, Directive (EU) 2015/412 amends it allowing for EU countries to prohibit or restrict GMOs that have been authorised or are under authorisation at EU level on wider grounds. These grounds that can be used by EU countries include town and country planning, land use, socio-economic impacts, co-existence* and public policy.

The amending directive also establishes the set of deadlines and responsibilities governing the decisions taken concerning the adjustment of the geographical scope of the authorisation, including a right to opt out based on new objective circumstances.

As of 3 April 2017, EU countries in which GMOs are cultivated have to introduce measures in border areas of their territory with the aim of avoiding possible cross-border contamination into neighbouring EU countries in which the cultivation of those GMOs is prohibited, unless such measures are unnecessary in the light of particular geographical conditions.

FROM WHEN DOES THIS DIRECTIVE APPLY?

It has applied since17 April 2001. EU countries had to incorporate it into their national law by 17 October 2002.

BACKGROUND

This directive is only one of the several building blocks of the EU’s legal framework for GMOs. The other building blocks are directives and regulations (focusing on issues like genetically modified food or transboundary movements of GMOs) that work to protect human and animal health and the environment, put in place harmonised procedures, and ensure the traceability of GMOs placed on the market.

KEY TERMS

Deliberate release: in the context of this legislation, any intentional introduction into the environment of GMOs without specific containment measures.

Genetically modified organisms: using techniques of modern biotechnology called gene technology, the genetic make-up of living cells and organisms can be modified. This allows man to breed plants and animals which can, for example, have a higher yield or resist disease.

Coexistence: the existence of genetically modified, conventional and organic crops requires rules to ensure that that they can be kept segregated from one another during cultivation, harvest, transport, storage and processing.

MAIN DOCUMENT

Directive 2001/18/EC of the European Parliament and of the Council of 12 March 2001 on the deliberate release into the environment of genetically modified organisms and repealing Council Directive 90/220/EEC - Commission Declaration (OJ L 106, 17.4.2001, pp. 1-39)

The successive amendments to Directive 2001/18/EC have been incorporated into the basic text. This consolidated version is of documentary value only.

Regulating GM crops: EU countries’ rights

SUMMARY OF:

WHAT IS THE AIM OF THE DIRECTIVE?

KEY POINTS

FROM WHEN DOES THIS DIRECTIVE APPLY?

BACKGROUND

KEY TERMS

MAIN DOCUMENT

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