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EP. Food safety: more transparency, better risk prevention

The EFSA Agency could request additional studies

Members of European Parliament (EP) want the European Food Safety Agency (EFSA) to publish safety studies before a product is authorised to go on to the market.

A proposal to allow the EFSA to work more efficiently and transparently was adopted by Parliament on Tuesday by 427 votes in favour, 172 against and 67 abstentions.

The revised rules aim to make risk assessment more transparent and ensure that the studies used by EFSA to authorise a product to be put on the market are reliable, objective and independent.

A new pre-submission procedure has been introduced, to allow the application process to be speeded up, as EFSA may provide advice to the applicant on how to provide all required information.

Additional studies to those submitted by companies

A common European Register of commissioned studies should be set up, to deter companies that are applying for authorisation from holding back unfavourable studies. If there is some doubt about the evidence provided by the companies, the agency could also consult third parties to identify whether other relevant scientific data or studies exist.

Parliament also agreed on a set of criteria to decide what kind of information can be kept confidential, eg the trademark under which a product will be marketed or detailed descriptions of preparations.

After the vote, rapporteur Renate Sommer (EPP, DE) stated that she cannot support the result of the vote and wants her name withdrawn from this file.

Background

The proposal is a follow-up to the European Citizens' Initiative on glyphosate, especially to concerns expressed in the initiative regarding the transparency of the scientific studies used to evaluate pesticides. It also follows a fitness check of the General Food Law, launched in 2014 and completed in January 2018 by the Commission.

Next steps

Parliament will now enter into negotiations with EU Ministers for a first reading agreement.

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