4 Amendments of Anna Maria CORAZZA BILDT related to 2010/2085(INI)
Amendment 5 #
Motion for a resolution
Recital E
Recital E
E. whereas the level of market surveillance differs considerably among Member States and a number of them fail to designate necessary resources for the efficient market surveillance and interpret ‘products posing serious risk’ differently, which can create barriers to the free movement of goods within the internal market;
Amendment 7 #
Motion for a resolution
Recital E a (new)
Recital E a (new)
Ea. Whereas the absence of efficient and proportionate market surveillance appears as one of the main reasons for unfair competition to legitimate and responsible market operators, especially SMEs;
Amendment 29 #
Motion for a resolution
Paragraph 5 a (new)
Paragraph 5 a (new)
5a. Calls upon the EU Member States to share product safety related inquiries and studies with other Member States. Reference numbers of concerned products should be included to facilitate product identification by other authorities, who could benefit from translating and using the information provided in the studies; calls upon Member States to allow their competent authorities to take market surveillance measures on the basis of test results or studies which have been delivered by other Member States in order to avoid duplication of works;
Amendment 32 #
Motion for a resolution
Paragraph 7
Paragraph 7
7. Urges the Commission to establish a public Consumer Product safety Information Database, which the RAMs Article 23 database might serve as a basis for, including a platform for complaints which will raise awareness of dangerous products across the borders in the internal market; calls for the establishment of a accident statistical system wherefrom mandatory annual reports will be published, coordinated and funded by the European Commission, where Member States shall report products that have caused accidents within their territoryinsists that careful attention must be paid in defining the rules of the use of the database and in developing key definitions in order to prevent negative collateral effects; calls on all Member States to join the Injury Database (IDB) so that information of health related incidents can be better coordinated at EU level; calls on the Member States to ensure that consumers are given the opportunity to complain of dangerous products to national authorities and that the complaints are looked into in an effective and professional manner;