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Initiative to limit industrial trans fats intakes in the EU

The main policy objectives of a possible regulation are: 1) to ensure a high level of health protection for EU consumers; 2) to contribute to reducing health inequalities, one the objectives of Europe 2020; 3) To contribute to the effective functioning of the Internal Market for foods that could contain industrial trans fats. Possible proposal should be available by the third quarter of 2017.
Website: http://ec.europa.eu/

REFIT Evaluation of the EU Legislation on Plant Protection Products and Pesticides Residues

The general objective of this Regulatory Fitness and Performance (REFIT) evaluation is to perform an evidence-based assessment of the implementation of the legislation on plant protection products and pesticides residues. The results of the evaluation will be the basis on which the Commission will draft the report to the European Parliament and the Council on the implementation of the plant protection products and pesticides residues legislation. The evaluation could be useful to improve the implementation on the EU rules on pesticides and might trigger legislative proposals in this policy area. For the purpose of this evaluation a consultation strategy will take place, with the involvement of Members of the Advisory Group for the Food Chain; with targeted stakeholders; with a survey for SMEs; with targeted consultations of authorities in the Member States and third countries; and with a public consultation to be published online.
Source: http://ec.europa.eu/

Roadmap – Commission’s Communication on a One-Health Action Plan to support Member States on Antimicrobial Resistance (AMR) Research Challenge

The Council conclusions of 17 June 2016 on AMR call for a reinforced EU strategy against AMR and a new and comprehensive EU Action Plan (AP) on AMR based on the One – Health approach. The current Action Plan has been subject to an evaluation, which showed that the EU can bring added value in the fight against AMR, by: 1) supporting Member States, particularly in establishing, implementing and monitoring their National Action Plans; 2) bringing together EU funds and instruments, to promote innovation and research against AMR; and 3) helping to strengthen the EU ‘s role in global fora, notably within the UN institutions and with major trade partners. The new AP should take the form of a Commission communication to the European Parliament and the Council. This action plan goes along the main propositions defended at a EuCheMS STOA workshop on AMR that took place earlier this year.
Website: http://ec.europa.eu/

Public Consultation on the Active Substance Benalaxyl

EFSA will assess all comments from interested parties regarding the active substance Benalaxyl. Input is requested on the following: physical/chemical properties; details of uses and further information; methods of analysis; mammalian toxicology; residues; and environmental fate and behavior.
Deadline: 25 January 2017
Website: http://www.efsa.europa.eu/