11 Amendments of Evelyne GEBHARDT related to 2009/0076(COD)
Amendment 107 #
Proposal for a regulation
Article 1 a (new)
Article 1 a (new)
Article 1a Precautionary principle This Regulation is based on the precautionary principle.
Amendment 108 #
Proposal for a regulation
Article 1 b (new)
Article 1 b (new)
Article 1b Aim of the Regulation The aim of this Regulation shall be a high level of health and environmental protection. Special attention shall be paid to protecting children, pregnant women and the sick.
Amendment 113 #
Proposal for a regulation
Article 7 – paragraph 1
Article 7 – paragraph 1
1. The applicant shall submit an application to include an active substance in Annex I, or to make subsequent amendments to the conditions of inclusion of an active substance, to the European Chemicals Agency (hereinafter referred to as 'the Agency') and inform it of. The Agency shall indicate the name of the competent authority of the Member State that heit has choosesn to evaluate histhe application. That competent authority (hereinafter referred to as 'the evaluating competent authority') shall be responsible for the evaluation of the application.
Amendment 114 #
Proposal for a regulation
Article 10 – paragraph 3
Article 10 – paragraph 3
3. Unless otherwise specified in the decision to renew the inclusion of an active substance in Annex I, the renewal shall be for an unlimited period of timeof the inclusion shall be reviewed after 10 years.
Amendment 123 #
Proposal for a regulation
Article 28
Article 28
Article deleted
Amendment 131 #
Proposal for a regulation
Article 44 – paragraph 3 – introductory part
Article 44 – paragraph 3 – introductory part
3. A biocidal product shall be considered as substantially identical to the reference product if one of the following conditions isare met:
Amendment 143 #
Proposal for a regulation
Article 54 – paragraph 3 – introductory part
Article 54 – paragraph 3 – introductory part
3. Every three years, starting in 2013, competent authorities shall submit to the Commission a report on the implementation of this Regulation in their respective territories. The report shall include:
Amendment 144 #
Proposal for a regulation
Article 54 – paragraph 3 – point b
Article 54 – paragraph 3 – point b
b) information on any poisonings involving biocidal products. and the possible health implications for vulnerable groups, such as children, pregnant women or the sick;
Amendment 145 #
Proposal for a regulation
Article 54 – paragraph 3 – point b a (new)
Article 54 – paragraph 3 – point b a (new)
Amendment 146 #
Proposal for a regulation
Article 54 – paragraph 3 – point b b (new)
Article 54 – paragraph 3 – point b b (new)
bb) information on possible measures to minimise risk and develop alternatives.
Amendment 147 #
Proposal for a regulation
Article 54 – paragraph 4
Article 54 – paragraph 4
4. The Commission shall draw up a report on the implementation of this Regulation and, in particular, on the functioning of the Community authorisation procedure and mutual recognition, by 1 January 202319 and every three years thereafter. The Commission shall submit the report to the European Parliament and the Council.