Activities of Csaba Sándor TABAJDI related to 2009/0076(COD)
Plenary speeches (1)
Placing on the market and use of biocidal products (debate)
Amendments (7)
Amendment 329 #
Proposal for a regulation
Article 31
Article 31
By way of derogation from Articles 25 and- 289, competent authorities of Member States may refuse mutual recognition of national authorisations granted for product types 15, 17 and 23 of Annex V provided that such a refusal can be justified on grounds of the protection of health of humans, particularly of vulnerable groups, the protection of health of animals or plants, the protection of environment national treasures possessing artistic, historic or archaeological value, or the protection of industrial and commercial property. Competent authorities of Member States shall without delay inform each other and the Commission of any decision taken in this respect and shall indicate the reasons thereof.
Amendment 420 #
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 implementation reports shall be annually published on the relevant website of the Commission. The report shall include:
Amendment 421 #
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 actions undertaken to lower the risk of future cases.
Amendment 430 #
Proposal for a regulation
Article 56 – paragraph 1 – introductionory part
Article 56 – paragraph 1 – introductionory part
1. The following information held by the competent authorities, the Agency or, as appropriate, the Commission on active substances shall be made, free of charge, publicly available in a single database, in a structured format at least on the relevant website of the Commission:
Amendment 431 #
Proposal for a regulation
Article 56 – paragraph 1 – point d a (new)
Article 56 – paragraph 1 – point d a (new)
(da) a clear reference if the active substance qualifies as persistent, bio- accumulative and toxic (PBT) or very persistent and very bioaccumulative (vPvB) in accordance with Annex XIII of Regulation (EC) No. 1907/2006 or as endocrine disrupter or if it has been classified in accordance with Regulation (EC) No 1272/2008 as one of the following: carcinogenic; mutagenic; neurotoxic; immunotoxic; toxic to reproduction; sensitising.
Amendment 465 #
Proposal for a regulation
Article 76 – paragraph 1
Article 76 – paragraph 1
Where, based on new evidence, a Member State has justifiable grounds to consider that a biocidal product, although satisfying the requirements of this Regulation, constitutes a serious risk to human or animal health or to the environment, particularly to vulnerable groups and to risk a failure of achieving the quality standards of Directive 2000/60/EC it may take appropriate provisional measures. The Member State shall without delay inform the Commission and the other Member States thereof and give reasons for its decision based on the new evidence.
Amendment 466 #
Proposal for a regulation
Article 76 – paragraph 2
Article 76 – paragraph 2